Литература к главе 3 и к приложениям 1, 2, 3, 4, 5, 6, 7, 9

552. Aird L., Bentall H. H., Roberts J. A. F. (1953). A relationship between cancer of stomach and the ABO group, Br. Med. J., 1, 799-801.

553. Albert E. D., Ваur М. Р., Mayr W. R. (eds.). Histocompatibility Testing 1984. Springer-Verlag, Berlin, Heidelberg, New York.

554. Allen F., Amos D. В., Bathelor R., Bodmer W., Ceppelini R., Dausset J., Engelfriet C., Jeannet M., Kissmeyer - Nielsen F., Morris P., Payne R., Terasaki P., vanRood J. J., Walford R" Zmijewski C., Albert E., Mattuiz P., Mickey M. R., Piazza A. (1970). Joint report of 4th Intern Histocompatibility Workshop, Histocompatibility testing (Terasaki P., ed.), Munksgaard, Kopenhagen, 17-47.

555. Allison A. C., Blumberg B. S. (1958). Domonance and recessivity in medical genetics, Am. J. Med. 25, 933-941.

556. Amos D. H., Kostyu D. D. (1980). HLA-A central immunological agency in man, Adv. in Hum. Genet, 10, 137-208.

557. Andreassen M. (1943). Haemofili i Danmark. Opera ex Domo Biologiae Hereditariae Humanae Universitatis Hafniensis Munksgaard, Vol. 6, Copenhagen.

558. Antonarakis S. E., Copeland K. L., Carpenter R. J. Jr., Carta С. A., Hoyer L. W, Caskey С. Т., Toole J. J., Kazazian H. H., Jr. (1985). Prenatal diagnosis of haemophilia A by factor VIII gene analysis, Lancet 1, 1407-1409.

559. Ball S. P., Cook P. J. L., Mars M., Buckton K. E. (1982). Linkage between dentinogenesis imperfacta and GC., Ann. Hun. Genet., 46, 35-40.

560. Baralle F. E., Shoulders С. С. (1984). Lipoprotein genes and hyperlipidemia, Schweiz. Med. Wschr., 114, 1351-1358.

561. Bateson W., Punnett R. G. (1908). Saunders: Confirmations and extensions of Mendel's principles in other animals and plants, Report to tee Evolution Committee of the Royal Society (London).

562. Bauer К. Н. (1927). Homoiotransplantation von Epidermis bei einei igen Zwillingen, Beitr. Klin. Chir., 141, 442-447.

563. Becker P. E. (1964). Myopathien. In: Becker P. E. (ed.), Humangenetik, ein kurzes Handbuch, Vol. III/I, pp. 411-550, Thieme, Stuttgart.

564. Becker P. E. (1953). Dystrophia musculorum progressiva, Thieme, Stuttgart.

565. Becker P. E. (1972). Neues zur Genetik und Klassifikation der Muskeldystrophien, Hum. Genet, 17. 1-22.

565a. Bell J. (1934). Huntington's chorea, Treasury of Human Inheritance 4.

566. Bell J. (1947). Dystrophia myotonica and allied diseases, Treasury of Human Inheritance 4, Teil V.

567. Benirschke K., Kim C. K. (1973). Multiple pregnancy, N. Engl. J. Med., 228, 1276-1284; 1329-1336.

568. Bennett T. (1975). The T-locus of the mouse, Cell, 6, 441-454.

569. Benzer S. (1957). The elementary units of heredity. In: McElroy W. D., Glass B. (eds.), The chemical basis of heredity, John Hopkins University Press, Baltimore, pp. 70-93.

570. Berg K. (1983). Genetics of coronary heart disease, Progr. Med. Genet., N. S., 5, 35-90.

571. Bernstein F. (1931). Zur Grundlegung der Chromosomentheorie der Vererbung beim Menschen, Z. Induktive Abstammungs-Vererbungslehre, 57, 113-138.

572. Bernstein F. (1930). Fortgesetzte Untersuchungen aus der Theorie der Blutgruppen, Z. Induktive Abstammungs-Vererbungslehre, 56, 233-237.

573. Bernstein F. (1930). Uber die Erblichkeit der Blutgruppen, Z. Induktiven Abstammungs-Vererbungslehre, 54, 400.

574. Bernstein F. (1925). Zusammenfassende Betrachtungen uber die erblichen Blutstrukturen des Menschen, Z. Induktive Abstammungs-Vererbungslehre, 37, 237.

575. Berwick D. M., Cretin S., Keeler E.B. (1980). Cholesterol, Children, and Heart Disease. An Analysis of Alternatives, Oxford, New York.

576. Bhende Y. M., Deshpande С. К., Bhata H. M., Sanger R., Race R. R., Morgan W. T. J., Watkins W.M. (1952). A "new" bloodgroup character related to the ABO system, Lancet, I, 903-904.

577. Bieber F. R., Nance W. E., Morton С. С., Brown J. A., Redwine F. O., Jordan R. L., Mohanakumar T. (1981). Genetic studies of an acardiac monster: Evidence of polar body twinning in man, Science, 213, 775-777.

578. Bilheimer D. W., Goldstein J. L., Grundy S. M., Starzl T. E., Brown M. S. (1984). Liver transplantation to provide low-density-lipoprotein receptors and low plasma cholesterol in a child with homozygous familial hypercholesterolemia, N. Engl. J. Med., 311, 1658-1664.

579. Birch-Jensen A. (1949). Congenital deformities of the upper extremities, Opera ex Domo Biologiae Hereditariae Humanae Universitatis Hafniensis Munksgaard, Kopenhagen, 19.

580. Blackburn H. (1979). Diet and mass hyperlipidemia: a public health view. In: Levy R., Rifkind В., Dennis В., Ernst N. (eds.), Nutrition, Lipids, and Coronary Heart Disease, Raven Press, New York.

581. Bodmer W. F. (1972). Population genetics of the HL-A System: Retrospect and prospect. In: Dausset J., Colombani J. (eds.), Histocompatibility testing, Munksgaard, Copenhagen, pp. 611-617.

582. Bodmer W. F., Bodmer J. G. (1978). Evolution and function of the HLA system, Br. Med. Bull., 34, 390-316.

583. Boman H., Ott J., Hazzard W. R., Albers J. J., Cooper M. N., Motulsky A. G. (1978). Familial hyperlipidemia in 95 randomly ascertained hyperlipidemic men, Clin. Genet., 13, 108.

584. Botstein D., White R. L., Skolnick M., Davis R. W. (1980). Construction of a genetic linkage map in man using restriction fragment length polymorphism, Am. J. Hum. Genet., 32, 314-331.

584a. Bowman B. H., Kurosky A. (1982). Haptoglobin: The evolutionary product of duplication, unequal crossing over, and point mutation. In: Harris H., Hirschhorn K. (eds.), Advances in Human Genetics, Vol. 12, Plenum Press, New York and London, pp. 189-261.

585. Boyd W. С. (1955). Maximum likelihood estimation of Rh gene frequencies in Pacific populations, Nature, 176, 648.

586. Boyd W. С. (1955). Simple maximum likelihood method for calculating Rh gene frequencies in Pacific populations, Am. J. Phys. Anthrop., 13, 447-453.

587. Bracken H. von (1934). Mutual intimacy in twins: Types of structure in pairs of identical and fraternal twins, Character and Personality, 2, 293-309.

588. Bridges C. B. (1936). The bar "gene", a duplication, Science, 83, 210.

589. Bridges R. A., Berendes H., Good R. A. (1959). A fatal granulomatous disease of childhood, Am. J. Dis. Child., 97, 387.

590. Bronnestam R. (1973a). Studies on the C3 polymorphism. Relation between phenotype and quantitative immunochemical measurements, Hum. Hered., 23, 128-134.

591. Bronnestam R. (1973b). Studies on the C3 polymorphism. Relationship between C3 phenotype and rheumatoid arthritis, Hum. He-red., 23, 206-213.

592. Brown M. S., Goldstein J. L., (1979). Abetalipoproteinemia. In: Goodman R. M., Motulsky A. G. (eds.), Genetic diseases among Ashkenazi Jews, Raven, New York.

593. Brown M. S., Goldstein J. L. (1984). How LDL receptors influence cholesterol and atherosclerosis, Sci. Am., 251, 58-66.

594. Brunzell J. D., Schrott H. G., Motulsky A. G., Bierman E. L. (1976). Myocardial infarction in the familial forms of hypertriglyceridemia, Metabolism, 25, 313-320.

595. Burke W. Hornung S., Copeland B. R., Furlong С. Е., Motulsky A. G. (1984). Red cell sodiumlithium countertransport in hypertension. In: Villarreal H., Sambhi M. P. (eds.), Topics in Pathophysiology of Hypertension, Martinus Nijhoff Boston, pp. 88-99.

596. Burke W., Motulsky A. G. (1985). Genetics of hypertension, Pract. Cardiol., 11, 159-173.

597. Burke W., Motulsky A. G. (1985). Hypertensionsome unanswered questions, JAMA, 253, 2260-2261.

598. Cagianit В., Rhyner K., Furrer W., Schnebli H. P. (1981). Thiosulfatesulphur transferase (Rhodanase) deficiency in Leber's hereditary optic atrophy, Lancet, II, 981-982.

599. Carney R. G., jr. (1976). Incontinentia pigmenti: A world statistical analysis, Arch. Dermatol., 112, 535-542.

600. Carter C. O. (1969). Genetics of common disorders, Brit. Med. Bull, 25, 52-57.

601. Carter C. O. (1961). The inheritance of congenital pyloric stenosis, Br. Med. Bull., 17, 251-254.

602. Canter C. O. (1976). Genetics of common single malformation, Br. Med. Bull., 32, 21-26.

603. Carter C. O. (1977). Genetic of common diseases. In: Geneenvironment interaction in common diseases, Japan Medical Research Foundation (ed.), pp. 108-117, University of Tokyo Press, Tokyo.

604. Caskey С. Т. (1985). New aid to human gene mapping, Nature, 314, 19.

605. Ceppellini R., Dunn L. C., Turri M. (1955). An interaction between alleles at the Rh locus in man which weakens the reactivity of the Rh₀ factor (Du), Proc. Natl. Acad. Sci. USA, 41, 283-288.

606. Ceppellini R. L., Siniscalco M. (1955). Una nuova ipotesi genetica per il sistema Lewissecretore e suoi reflessi nei reguardi di alcune evidenze di linkage con altri loci, Riv. 1st. sieroter Ital, 30, 431-445.

607. Ceppellini R., Siniscalo M., Smith С. А. В. (1955/56). The estimation of gene frequencies in a randommating population, Ann. Hum. Genet., 20, 97.

608. Chakravartti M. R., Vogel F. (1973). Topics in human genetics, Vol. I, A twin study on leprosy, Thieme, Stuttgart.

609. Chown В., Lewis M., Hiroko K. (1957). A "new" Kell blood group phenotype, Nature, 180, 711.

610. Chung C. S., Morton N. E. (1959). Discrimination of genetic entities in muscular dystrophy, Am. J. Hum. Genet., 11, 339-359.

611. Cloninger C.R., Rice J., Reich Th., McGrif-fin P. (1982). Genetic analysis of seizure disorders as multidimensional threshold characters. In: Anderson V. E. (ed.), Genetic basis of the epilepsies, Raven Press, New York, pp. 291-309.

612. Cohen-Hagenauer O., Robbins E., Messart C., Busson M., Deschamps I., Hors J., Lalouel J.-M., Dausset J., Cohen D. (1985). A systematic study of HLA class II-β DNA restriction fragments in insulindependent diabetes mellitus, Proc. Natl. Acad. Sci. USA, 82, 3335-3339

612a. Coneally P. M., Rivas M. L. (1980). Linkage analysis in man, Adv. in Hum. Genet., 10, 209-266.

612b. Cook P. J. L., Robson E. В., Buckton К. Е., Jacobs P. A., PolaniP. E. (1974). Segregation of genetic markers infamilies with chromosome polymorphisms and structural rearrangements involving chromosome 1, Ann. Hum. Genet., 37, 261-274.

613. Carney G., Seedburgh D., Thompson В., Campbell D. M., Mac Gillivray I., Timlin D. (1979). Maternal Height and Twinning, Ann. Hum. Genet., 43, 55-59.

614. Cudworth A. G., Wolf E. (1982). The genetic susceptibility to type I (insulin-dependent) diabetes mellitus, Clin. Endocr. Metab., 11, 389-408 1.

615. Cuenot L. (1905). Les races pures et leur combinaisons chez les souris, Arch. Zool. Exp. Genet., 3, 123-132.

616. Czeizel A. (1978). The Hungarian congenital malformation monitoring system, Acta Paediat. Academ. Scientiarum Hungaricae, 19, 225-238.

617. Czeizel A., Kiss P., Oszotovics M. et al. (1978). Nationwide investigations of multiple malformations, Acta Paediat Academ. Scientiarum Hungaricae, 19, 275-280.

618. Czeizel A., Pazonyi I., MetrekiJ., Tomka M. (1979). The first five years of the budapest twin register, 1970-1974, Acta Genet. Med. Gemellol, 28, 73-76.

619. Czeizel A., Tusnddy G., Vaczo G., Vizkelety T. (1975). The mechanism of genetic predisposition in congenital dislocation of the hip, J. Med. Genet, 12, 121-124.

620. Dalgaard O. Z. (1957). Bilateral polycystic disease of the kidneys, Opera ex Domo, Biologiae Hereditariae Humanae Universitatis hafniensis Munksgaard, Copenhagen, 38, 255 pp.

621. Das N. K., Biro P. A., Duceman В., Sood A. K., Shyma E., Reddy P., Lawrance S., Pan J., Weissman S. M. (1983). Molecular studies of the genes of the human major histocompatibility. In; Caskey С. Т., White R. L. (eds.), Banbury Report 14, Cold Spring Harbor Lab., p. 41-51.

622. Dausset J., Colombani J. (1972). Histocompatibility testing 1972, Munksgaard, Copenhagen.

623. Dausset J., Contu L. (1980). The MHC and immune response in man, Progr. Immunol., 4, 513-529.

624. Davies K. E., Young B. D., Elles R. G., Hill M. E., Williamson R. (1981). Cloning of a representative genomic library of the human X chromosome after sorting by flow cytometry, Nature, 293, 374-376.

625. Davis S. H., Gavin J., Goldsmith K. L. G., Graham J. В., Hamper J., Hardisty R. M., Harris J. В., Holman C. A., Ingram G. I. C., Jones T. G., McAfee L. A., McKusick V. A., O'Brien J. R., Race R. R., Sanger R., Tippett P. (1963). The linkage relations of hemophilia A and hemophilia В (christmas disease) to the Xg blood group system, Am. J. Hum. Genet, 15, 481-492.

626. Deeb S. S., Motulsky A. G., Albers J. J. (1985). A partial cDNA clone for human apolipoprotein B, Proc. Natl. Acad. Sci. USA, 82, 4983-4986.

627. Degnbol В., Green A. (1978). Diabetes mellitus among first- and second-degree relatives of early onset diabetics, Ann. Hum. Genet., 42, 25-47.

628. Demenais F., Bonaiti C., Briard M.-L., Feingold J., Fr'ezal J. (1979). Congenital glaucoma: Genetic models, Hum. Genet., 46, 305-317.

629. Domahue R. P., Bias W. В., Renwick J. H., McKusick V. A. (1968). Probable assignment of the Duffy bloodgroup locus to chromosome 1 in man. Proc. Natl. Acad. Sci. USA, 61, 949.

630. Dorn H. (1959). Xeroderma pigmentosum, Acta Genet. Med. Gemellol (Roma), 8, 395-408.

631. Dungern E. von, Hirzfeld L. (1911). Uber gruppenspezifische Structuren des Blutes. III. Z. Immunitatsforsch., 8, 526-562.

632. DunsfordI., Bowley C. C., Hutchinson A. M., Thompson J. S., Sanger R., Race R. R. (1953). A human bloodgroup chimera, Br. Med. J., II, 81.

633. Dupont В., Smithwick E. M., Oberfield S. E., Lee T.-D., Levine L.S. (1977). Close genetic linkage between HLA and congenital adrenal hyperplasia (21-hydroxylase deficiency), Lancet, II, 1309-1312.

634. Eaves L. J. (1982). The utility of twins. In: Anderson V. E. et al. (eds.), Genetic basis of the epilepsies, Raven Press, New York, pp. 249-276.

635. Eder H. A., Gidez L. J. (1982). The clinical significance of the plasma high density lipoproteins, Med. Clin. North Am., 66, 431-440.

636. Edwards J. H. (1960). The simulation of mendelism, Acta Genet., (Basel), 10, 63-70.

637. Edwards J. H. (1965). The meaning of the associations between blood group and disease, Am. J. Hum. Genet., 29, 77.

638. Edwards J. A., Gale R. P. (1972). Camptobrachydactyly: A new autosomal sominant trait with two probable homozygotes, Amer. J. Hum. Genet., 24, 464-474.

639. Egger J., Wilson J. (1983). Mitochondrial inheritance in a mitochondrially mediated disease, New England Journal Med., 309, 142-146.

640. Ehling U. H. (1966). Dominant mutations of the skeleton in off spring of X-irratiated male mice, Genetics, 54, 1381-1389.

641. Ehling U. H. (1970). Evaluation of presumed dominant skeletal mutation. In: Vogel F., Rohrborn G. (eds.), Chemical mutagenesis in mammals and man, Springer, Berlin, Heidelberg, New York, pp. 162-166.

642. Ehling U. H., Randolph M. L. (1962). Skeletal abnormalities in the F₁ generation of mice exposed to ionizing radiations, Genetics, 47, 1543-1555.

643. Eichwald E. J., Silmser C. R. (1955). Communication, Transplant. Bull., 2, 148-149.

644. Ellison R. T. III, Kohler P. F., Curd J. G., Judson F. N., RellerL.B. (1983). Prevalence of congenital or acquired complement deficiency in patients with sporadic meningococcal disease, N. Engl. J. Med., 308, 913-916.

645. Elsas L. J., Endo F., Strumlauf E., Elders J., Priest J. H. (1985). Leprechaunism: a inherited defect in a highaffinity insulin receptor, Am. Hum. Genet., 37, 73-88.

646. Elston R. C. (1979). Major locus analysis for quantitative trains, Amer. J. Hum. Genet., 31, 655-661.

647. Elston R. C. (1981). Segregation analysis, Adv. in Hum. Genet., 11, 63 120.

648. Elston R. C., Glassman E. (1967). An aproach to the problem of whether clustering of functionally related genes occurs in higher organisms, Genet. Res. (London), 9, 141-147.

649. Elston J. H., Lange K. (1975). The prior probability of autosomal linkage, Ann. Hum. Genet., 38, 341-350.

650. Epstein F. H. (1976). Genetics of ischemic heart disease, Postgrad. Med., J., 52, 477-480.

651. Eriksson S. (1965). Studies in alpha 1-antitrypsin deficiency, Acta Med. Scand., 177, 175.

652. Erlich H., Stetler D., Grumet С (1983). Restriction length polymorphism analysis of HLA-typed families using cloned HLA probes. In: Caskey С. Т., White R. L. (Eds.), Banbury Report 14, Cold Spring Harbor Lab., pp. 327-334.

653. Fagerhol M. K., Cox D. W. (1981). The Pi polymorphism: Genetics, biochemical and clinical aspects of human alpha t-antitrypsin, Adv. in Hum. Genet, 11, 1-62.

654. Falconer D. S. (1965). The inheritance of liability to certain diseases, estimated from the incidence among relatives, Ann. Hum. Genet., 29, 51.

655. Falconer D. S. (1967). The inheritance of liability to diseases with variable age of onset with particular reference to diabetes mellitus, Ann. Hum. Genet, 31, 1-20.

656. Farabee (1905). Inheritance of digital malformations in man, Papers of the Peabody Museum for Americal Archeology and Ethnology (Harvard University), 3, 69.

657. Farhud D. В., Ananthakrishnan R., Walter H. (1972). Association between the C3 pheno-types and various diseases, Hum. Genet., 17, 57-60.

658. Farquhar J. W, Maccoby N., Wood P. D., Alexander J. K., Breitrose H., Brown B. W. ir., Haskell W. L., McAlister A. L., Meyer A. J., Nash J. D., Stern M. P. (1977). Community education for cardiovascular health, Lancet, 1, 1192-1195.

659. Felle W. (1950). An introduction to probability theory and its applications, John Wiley and Sons, New York.

660. Ferns G. A. A., Stocks J., Ritchie C., Galton D. J. (1985). Genetic polymorphisms of apolipoprotein C-III and insulin in survivors of myocardial infarction, Lancet, 2, 300-303.

661. Fialkow P. J., Giblett E. R., Motulsky A. G. (1967). Measurable linkage between ocular albinism and Xg, Am. J. Hum. Genet., 19, 63-69.

662. Finkelstein S., Walford R. L., Myers L. W., Ellison G. W. (1974). HL-A antigens and hypersensitivity to brain tissue in multiple sclerosis, Lancet, I, 736.

663. Finney D. J. (1947/9). The truncated binomial distribution, Ann. Eugen., 14, 319-328.

664. Fischer R. A. (1918). The correlation between relatives on the supposition of Mendelian inheritance, Trans. R. Soc. (Edinburgh), 52, 399-433.

665. Fischer R. A., Race R. R. (1946). Rh gene frequencies in Britain, Nature, 157, 8.

666. Floderus Y., Iselius L., Lindsten J., Wetterburg L. (1982). Evidence for a major locus as well as a multifactorial component in the regulation of human red blood cell catechol-O-methyltransferase activity, Hum Hered., 32, 76-79.

667. Folstein S. E., Phillips J. A. Ill, Meyers D. A., Chase G. A., Abbott M. H., Franz M. L., Waber P. G., Kazazian H. H. Jr., Conneally P. M., Hobbs W., Tanzi R., Faryniarz A., Gibbons K., Gussella J. (1985). Huntington's disease: two families with differing clinical features show linkage to the G8 probe, Science, 229, 776-779.

668. Franceschetti A., Klein D. (1957). Two families with parents of different types of red-green blindness, Acta Genet. (Basel), 7, 255.

669. Fraser G. R. (1976). The cause of profound deafness in childhood, Johns Hopkins University Press, Baltimore, London.

670. Fraser G. R., Friedman A. I. (1967). The causes of blindness in с chindhood, Johns Hopkins University Press, Baltimore.

671. Fredrickson D. S., Goldstein J. L., Brown M. S. (1978). The familian hyperlipoproteinemias. In: Stanbury J. В., Wyngaarden J. В., Fredrickson D. S. (eds.), The Metabolic Basis of Inherited Disease, 4th ed., McGraw-Hill, New York, pp. 604-655.

672. Fuhrmann W. (1963). Das Syndrom der erblichen Nephropathy mit Innenohrschwerhorigkeit (Alport-Syndrom), Dtsch. Med, Wochenschr., 88, 525-532.

673. Fuhrmann W. (1974). Die formale Genetik des Menschen. In: Vogel F. (ed.), Handbuch der Allgemeinen Pathologie, Vol. IX, Erbgefuge, Springer, Berlin, Heidelberg, New York, pp. 147-259.

674. Fuhrmann W., Stahl A., Schroeder T.M. (1966). Das orofaciodigitale Syndrom, Humangenetik, 2, 133-164.

675. Gallon F. (1876). The history of twins as a criterium of the relative powers of nature, J. Anthropol. Inst.

676. Gartler S. M., Francke U. (1975). Half chromatid mutations: Transmission in humans? Am. J. Hum. Genet., 27, 218-223.

677. Gaul L. E. (1953). Heredity of multiple benign cystic epithelioma, Arch. Dermatol. Syph. (Chicago), 68, 517.

678. Gelb A. F., Klein E., Lieberman J. (1977). Pulmonary function in nonsmoking subjects with alpha t antitrypsin deficiency (MZ phenotype), Am. J. Med., 62, 93.

679. Gerard G., Vitrac D., Le Pendu J., Muller A., Oriol R. (1982). H-deficient blood groups (Bombay) of Reunion island, Amer. J. Hum. Genet, 34, 937-947.

680. Gesell A., Thompson H. (1929). Learning and growth in identical infant twins: An experimental study by the method of co-twin control, Genet. Psychol. Monogr., 6, 5-124.

681. Geyer E. (1940). Ein Zwillingsparchen mit zwei Vatern. Arch. Rassenbiol., 34, 226-236.

682. Giblett E. R., Klebanoff S. J., Pincus S. H., Swanson J., Park В. H., McCullough J. (1971). Kell phenotypes in chronic granulomatous disease: a potential transfusion hazard, Lancet, I, 1235.

683. Goldberg A. S. (1978). Pitfalls in the resolution of I. Q. inheritance, pp. 195-222, In: Morton N. E., Chung С S. (eds.), Genetic epidemiology, Academic Press, New York etc.

684. Goldstein J. L., Brown M. S. (1977). Atherosclerosis: thelowdensity lipoprotein receptor hypothesis, Metabolism, 26, 1257-1275.

685. Goldstein J. L., Brown M. S. (1979). LDL receptor defectin familial hypercholesterolemia, Med. Clin. North Am., 66, 335-362.

686. Goldstein J. L., Hazzard W. R., Schrott H. G., Bierman E. L., Motulsky A. G. (1973). Hyper-lipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, J. Clin Invest., 54, 1544-1568.

687. Grebe H. (1959). Erblicher Zwergwuchs, Ergeb. Inn. Med. Kinderheilkd., 12, 343-427.

688. Greiner J., Schleiermacher E., Smith Т., Len-hard V., Vogel F. (1978). The HLA system and leprosy in Thailand, Hum. Genet., 42, 201-213.

688a. Greiner J., Kruger J., Palden L., Jung E. G., Vogel F. (1983). A linkage study of acrokeratoelastoidosis, Possible mapping to chromosome 2, Hum. Genet., 63, 222-227.

689. Grosse-Wilde H., Bertrams J., Schuppien W., Netzel В., Ruppelt W., Kuwert E.K. (1977). HLA-D typing in 111 multiple sclerosis patients: Distribution of four HLA-D alleles, Immunogenetics, 4, 481-488.

690. Gruneberg H. (1952). Ouasi-continuous variations in the mouse, Symp. Genet, 3, 215-227.

691. Gruneberg H. (1952). Genetical studies in the skeleton of the mouse. IV. Ouasicontinuous variations, J. Genet, 51, 95-114.

692. Girzeschik K.-H. (1973). Utilization of mosaic cellhypbrids for genetic studies in man, Hum. Genet, 19, 1-40.

693. Gusella J. F., Tanzi R. E., Anderson M. A., Hobbs W., Gibbons K., Raschtchian R., Gilliam T. С, Wallace M. R., Wexler N. S., Conneally P.M. (1984). DNA markers for nervous system diseases, Science, 225, 1320-1326.

694. Gusella J. F., Wexler N. S., Conneally P. M., Naylor S. L., Anderson M. A., Tanzi R. E., Watkins P. C., Ottina C., Wallace M. R., Sakaguchi A. Y, Young А. В., Shoulson I., Bonilla E., Martin J. B. (1983). A polymorphic DNA marker genetically linked to Huntington's disease, Nature, 306, 234-238.

695. Haase F. H. (1938/39). Die Ubersterblichkeit der Knaben als Folge recessiver geschlechtsgebundener Anlagen, Z. Menschl. Vererbungs-Konstitutionslehre, 22, 105-126.

696. Hadorn E. (1955). Developmental genetics and lethal factors, John Wiley and Sons, London, New York.

697. Haldane J. B. S. (1941). The relative importance of principal and modifying genes in determining some human diseases, J. Genet., 41, 149-157.

698. Haldane J. B. S., Smith С. А. В. (1947/9). A simple exact test for birth order effect, Ann. Eugen., 14, 116-122.

699. Haldane J. B. S., Smith C. A. B. (1947). A new estimate of the linkagebetween the genes for color blindness and haemophilia in man, Ann. Eugen., 14, 10-31.

700. Hall J. G., Dorst J. P., Taybi H, Scott С. I., hanger L. O., McKusick V.A. (1969). Two probable cases of homozygosity for the achondroplasia gene, Birth Defects, 4, 24-34.

701. Hamby R. I. (1981). Hereditary aspects of coronary artery disease, Am. Heart. J., 101, 639-649.

702. Harris H. (1970). Cell fusion, Clarendon, Oxford.

702a. Harris H. (1948). A sex-limiting modifying gene in diaphyseal aclasis (multiple exostoses), Ann. Eugen, 14, 165-170.

703. Harris H, Smith C.A.B. (1948). The sib-sib age of onset correlation among individuals suffering from a hereditary syndrome produced by more than one gene, Ann. Eugen, 14, 309-318.

704. Hatzold O. (1966). Die Sexualproportion der Geborenen und ihre Schwankungen als prakonzeptionelles Wahrscheinlichkeitsproblem, Dtsch. Akad. f Bevolkerungswissenschaft, Reihe В., Vol. 5.

705. Hauge M., Harvald В., Fischer M., Gottlieb-Jensen K., Juel: nielsen N., Raebild I., Shapiro R., Videbech T. (1968). The Danish twin register, Aota Genet. Med. Gemellol (Roma), 18, 315-332.

706. Havel R. J. (1982). Familial dysbetalipo-proteinemia, Med. Clin. North Am., 66, 441-454.

707. Haverkamp-Begemann N., Lookeren-Campagne van A (1952). Homozygous from of Pelger Huet's nuclear anomaly in man, Acta Haematol (Basel), 7, 295-303.

708. Haws D. V., McKusick V.A. (1963). Farabee's brachydactylous kindred revisited, Johns Hopkins Med. J., 113, 20-30.

709. Hegeman J. P., Mash A. J., Spivey B.E. (1974). Genetic analysis of human visual parameters in populations with varying incidence of strabism, Am. J. Hum. Genet., 26, 549-562.

710. Helmbold W. (1959). Ober den moglichen Aufbau des Rh-Genkomplexes, Blut, 5, 141-148.

711. Helmbold W., Prokop O. (1958). Die Bestimmung der ABO-Genfrequenzen mittels der maximum-likelihood-Methode und anderer Verfahren anhand forensischer Blutgruppen-bestimmungen in Berlin, Blut, 4, 190-201.

712. Hershon K., Brunzell J., Albers J. J., Haas L., Motulsky A. (1981). Hyper-apo-B-lipoproteinemia with variable lipid phenotype (familial combined hyperlipidemia). Arterosclerosis, 1, 380a.

712a. Hirszfeld L. (1928). Konstitutionsserologie und Blutgruppenforschung, Springer, Berlin.

713. Hitman G. A., Jowett N. I., Williams L. G., Humphries S., Winter R. M., Galton D. J. (1984). Polymorphism in the 5'-flamking region of the insulin gene and non-insulin-dependent diabetes, Clin. Sci., 66, 383-388.

714. Hitzig W. H., Seger R. A. (1983). Chronic granulanatous disease, a heterogenous syndrome, Hum. Genet, 64, 207-215.

715. Holmes В., Quie P. G., Windhorst D. В., Good R. A. (1966). Fatal granulomatous disease of childhood: an inborn abnormality of phagocytic function, Lancet, I, 1225.

716. Howell-Evans W., McConnel R. B., Clarke С. A., Sheppard P.M. (1958). Carcinoma of the oesophagus with keratosis palmaris and plantaris (tylosis), Q. J. Med, (new series), 27, 413-429.

717. Hrubec Z., Robinette C. D. (1984). The study of human twins in medical research, N. Engl. J, Med, 310, 435-441.

718. Hully S. B., Rosenman R. H., Bawol R. D., Brand R. J. (1980). Epidemiology as a guide to clinical decisions. The association between triglyceride and coronary heart disease, N. Engl. J. Med, 302, 1383-1389.

719. Humphries S. E., Kessling A. M., Horsthemke В., Donald J. A., Seed M., Jowett N., Holm M., Galton D. J., Wynn V., Williamson R. (1985). A common DNA polymorphism of the low-density lipoprotein (LDL) receptor gene and its use in diagnosis, Lancet, 1, 1003-1005.

720. Hulten M. (1974). Chiasma distribution at diakinesis in the normal human male, Hereditas, 76, 55-78.

721. Husen T. (1959). Psychological twin research, Almquist and Wiksell, Stockholm.

722. Illingworth D. R., Sexton G. J. (1984). Hypocholesterolemic effects of mevinolin in patients with heterozygous familial hyperholesterolemia, J. Clin. Invest, 74, 1972-1978.

723. Inkeles S., Eisenberg D. (1981). Hyperlipidemia and coronary atherosclerosis: a review, Medicine, 60, 110-123.

724. Iselius L., Lalouel J. M. (1982). Complex segregation analysis of hyperalphalipoproteinemia, Metabolism, 31, 521-523.

725. Jackson J. F., Currier R. D., Terasaki P. I., Morton N. E. (1977). Spinocerebellar ataxia and HLA linkage. Risk prediction by HLA typing, N. Engl. J. Med., 296, 1138-1141.

726. Johannsen W. (1909). Elemente der exakten Erblichkeitslehre, G. Fischer (3rd ed., 1926), Jena.

727. Johnson B. C., Epstein F. H., Kjelsberg M. O. (1965). Distribution and familial studies of blood pressure and serum cholesterol levels in a total community - Tecumseh, Michigan, J. Chron. Dis., 18, 147.

728. Jorgensen G. (1974). Erbfaktoren bie haufigen Krankheiten. In: Vogel F. (ed.), Handbuch der allgemeinen Pathologie, Vol. IX, Erbgefuge, Springer, Berlin, Heidelberg, New York, pp. 581-665.

729. Kaelin A. (1955). Statistische Pruf - und Schatzverfahren fur die relative haufigkeit von Merkmalstragern bei einem der Auslese unterworfenen Merkmal mit Anwendung auf das Retinagliom, Arch. Julius Klaus Stiftung Vererbungsforsch., 30, 263-485.

729a. Kampe O., Larhammer D., Wiwan K., Scheming L., Claesson L.,Gustafsson K., Paabo S., Hyldig - Nielsen J. J., Rask L., Peterson P. A. (1983). Molecular analysis of MHC antigens. In: Moller E., Moller G. (eds.), Genetics of the immune response, Plenum, 001 York, pp. 61-79.

730. Kagan A., Rhoads G. C., Zeegan P. D., Nichaman M. Z. (1971). Coronary heart disease among men of Japanese ancestry in Hawaii: the Honolulu heart study, Isr. J. Med., Sci., 7, 1573.

731. Kallmann F. J. (1938). The genetics of schizophrenia, Augustin, New York.

732. Kallmann F. J. (1946). The genetic theory of schizophrenia. An analysis of 691 schizophrenic twin index families, Am. J. Psychiatry, 103, 3.

733. Kan Y. W., Dozy A. M. (1978). Antenatal diagnosis of sicklecell anaemia by DNA analysis of amnioticfluid cells, Lancet, II, 910-912.

734. Kannell W. B. (1976). Some lessons in cardiovascular epidemiolog from Framingham, Am. J. Cardiol., 37, 268-282.

735. Keats B. J. В., Morton N. E., Rao D. C., Williams W. (1979). A sourse book for linkage in man, Johns Hopkins Univ. Press, Baltimore.

736. Keats J. В., Morton N. E., Rao D. C. (1981). Reduction of physical assigment to a standard lod table: Chromosome 1, Hum. Genet., 56, 353-359.

737. Kelley W. N., Greene M. L., Rosenbloom F. M., Henderson J. F., Seeqmiller J. E. (1969). Hy-poxanthineguanine phosphoribosyltranspherase deficiency in guut, Ann. Intern. Med., 70, 155.

738. Kiekebusch-Muller B. D., Arnold H., Mayr W. R. (1980). Ein Algorithmus zur Berechnung der HLA-Haplotypfrequenzen (an algorhithm for calculating HLA haplotype frequencies), Anthrop. Anzeiger, 38, 1-10.

739. Kissmeyer-Nielsen F. (ed.) (1975). Histocompatibility testing 1975, Munkagaard, Copenhagen.

740. Klein J. (1974). Genetic polymorphism of the histocompatibility 2 loci of the mouse, Ann. Rev. Genet., 8, 63-77.

741. Klein J. (1975). Biology of the mouse histocompatibility-2 complex, Springer, Berlin, Heidelberg, New York.

742. Kloimwieder R. (1942). Die Intelligenz in ihren Beziehungen zur Vererbung, Umwelt Ubung, Z. Menschl. Vererbungs - Konstitutionslehre, 25, 582-617.

743. Knowler W. C., Pettit D. J., Vasquez В., Rotwein P. S. Andreone T. L., Permutt M. A. (1984). Polymorphism in the 5'flanking region of the human insulin gene, J. Clin. Invest., 74, 2129-2135.

744. Koller S. (1940). Methodik der menschlichen Erbforschung II. Die Erbstatistik in der Familie. In: Just G., Bauer К. Н., Hanhart E., Lange J. (eds.), Handbuch der Erbbiologie des Menschen, Vol. II, Methodik, Genetik der Gesamtperson, Springer, Berlin, pp. 261-284.

745. Kravitz K., Skolnick M., Edwards C., Cartwright G., Amos В., Carmelli D., Baty B. (1978). Pedigree analysis of the linkage between HLA and hemochromatosis. In: Morton N. E., Chung C. S. (eds.), Genetic epidemiology, Academic Press, New York, pp. 241-246.

746. Krtiger J. (1973). Zur Unterscheidung zwischen multifaktoriellen Erbgang mit Schwellenwerteffekt und einfachen diallem Erbgang, Hum. Genet., 17, 181-252.

747. Kriiger J., Propping P. (1976). Ruckgang der Zwillingsgeburten in Deutschland, Dtsch. Med. Wochenschr., 101, 475-480.

748. Kruger J., Vogel F. (1975). Population genetics of unequal cros sing over, J. Mol. Evol, 4, 201-247.

749. Kueppers F. (1975). α₁-Antitrypsin. In: Becker P. E. (ed.), Humangenetik, ein kurzes Handbuch, Vol. 1/3, Thieme, Stuttgart, pp. 35-49.

750. Kunkel L. M., Tantravahi U., Eisenhard M., Latt S. (1978). Regional localization on the human X of DNA segments cloned from flow sorted chromosomes, Nucleic Acid Res., 10, 1557-1578.

751. Kurachi K., Chandra Т., Degen S.J., White Т. Т., Marchioro T. L., Woo S. L. C., Davie E.W, (1981). Cloning and sequence of cDNA coding for alpha-antitrypsin, Proc. Natl. Acad. Sci. USA, 78, 6826-6830.

752. Lalouel J. M., Morton N. E., MacLean C. J., Jackson J. (1977). Recurrence risk in complex inheritance with special regard to pyloric stenosis, J. Med. Genet., 14, 408-414.

753. Landsteiner K., Wiener A. S. (1940). An agglutinable factor in human blood recognized by immune sera for rhesus blood, Proc. Soc. Exp. Biol. Med., 43, 223.

754. Lange K., Boehnke M. (1982). How many polymorphic genes will it take to span the

human genome? Amer. J. Hum. Genet., 34, 842-845. 754a. Lange K., Page B.M., Elston R.C. (1975). Age trends in human hiasma frequencies and recombination fractions. I. Chiasma frequencies, Am. J. Hum. Genet., 27, 410-418.

755. Laurell С. В., Eriksson S. (1963). The electrophoretic ах-globulin pattern of serum alantitrypsin deficiency, Scand. J. Clin. Lab. Invest., 15, 132.

756. Lemser H. (1938). Zur Erb- und Rassenpathologie des Diabetes mellitus, Arch. Rassenbiol., 32, 481.

757. Lenz F. (1923). Ubersterblichkeit der Knaben im Lichte der Erblichkeitslehre, Arch. HyG., 93, 126-150.

757a. Lenmark A. (1985). Molecular biology of type 1 (insulin-dependent) diabetes mellitus, Diabetes, 28, 195-203.

758. Lenz W. (1959). Ursachen des gesteigerten Wachstums der heutigen Jugend. In: Akzeleration und Ernahrung Fettlosliche Wirkstoffe, Vol. 4.

759. Lenz W. (1961). Zur Genetik der Incontinentia pigmenti, Ann. Paediatr. (Basel), 196, 141.

760. Lenz W. (1975). Half chromatid mutations may explain incontinentia pigmenti in males, Am. J. Hum. Genet, 27, 690-691.

761. Lenz W. (1973). Vererbung und Umwelt bie der Entstehung von Missbildungen, Uuman-biologie, 121, 132-145.

762. Levine P., Stetson R. E. (1939). An unusual case of intragroup agglutination, J. Am. Med. AssoC., 113, 126-127.

763. Levy R. I. (1981). Declining mortality in coronary heart disease, Arteriosclerosis, 1, 312-325.

764. Lewis E. В. (1951). Pseudoallelism and gene evolution, Cold Spring Harbor Symp. Quant. Biol, 16, 159-174.

765. Lieberman R., Humphrey W., (1972). Association of the H-2 type with genetic control of immune responsiveness to (v2a) allotypes in the mouse, J. Exp. Med., 136, 1222-1230.

766. Lilly F. (1966). The inheritance of susceptibility to the Gross leukemia virus in mice, Genetics, 53, 529-539.

767. Lundsgaard R. (1944). Leber's disease. A genealogiC., genetic and clinical study of 101 cases of retrobulbar optic neuritis in 20 Danish families, Acta Ophthalmol. /Suppl/ (Kbh.), 30.

768. Luxenburger H. (1935). Untersuchungen an schizophrenen Zwillingen und ihren Geschwistern zur Prufung der Realitat von Manifestationsschwankungen, Z. Gesamte Neurol. Psychiat, 154, 351-394.

769. Luxenburger H. (1940). Zwillingsforschung als Methode der Erbforschung beim Menschen. In: Just G, Bauer K. H., Hanhart E., Lange J. (eds.), Handbuch der Erbbiologie des Menschen, Vol. II, Methodik, Genetik der Gesamtperson, Springer, Berlin, pp. 213-248.

770. Maartmenn-Moe K., Magnus P., Golden W., Berg K. (1981). Genetics of the low density lipoprotein receptor: III. Evidence for multiple normal alleles at the low density lipoprotein receptor locus, Clin. Genet., 20, 113-129.

771. Maartmann-Moe K., Magnus P., Borresen A.-L., Berg K. (1981). Low density lipoprotein receptor activity in cultured fibroblasts from subjects with or without ischemic heart disease (in the ab sence of familial hypercholesterolemia), Clin. Genet., 20, 337-346.

772. Madlener M. (1928). Eine Bluterfamilie, Arch. Rassenbiol., 20, 390-394.

773. Mann J. D., Cahan A., Gelb A., Fischer N., Hamper J., Tipett P., Sanger R., Race R.R. (1962). A sex-linked blood group, Lancet, I, 8.

774. Maroteaux P. (1974). Les maladies esseuses de l'enfant, Flammarion, Paris.

775. Marsh D. G., Meyers D. A., Bias W. B. (1981). The epidemiology and genetics of atopic allergy, New Engl. J. Med., 305, 1551-1559.

776. Marsh W. L. (1978). Chronic granulomatous disease, Kx antigen and the Kell blood groups. In: Brewer G. J. (ed.), Progress in clinical and biological research. The red cell, Vol. 21, Liss, New York, pp. 493-507.

777. Marsh W. L., Oyen R., Nichols M. E., Allen F. H. (1975). Chronic granulomatous dosease and the Kell blood groups, Br. J. Haematol., 29, 247.

778. Massart C., Busson M., Deschamps I., Hors J., Lalouel J.-M., Dausset J., Cohen D. (1985). A systematic study of HLA class II-β DNA restriction fragments in insulin-dependent diabetes mellitus, Proc. Natl. Acad. Sci. USA, 82, 3335-3339.

779. Matthiuz P. L., Ihde D., Piazza A., Ceppelini R., Bodmer W.F. (1970). New Approaches to the population genetics and segregation analysis of the HL-A system. In: Terasaki P. (ed.), Histocompatibility Testing, Munksgaard, Kopenhagen, pp. 193-205.

780. Maynard-Smith S., Penrose L. S., Smith С. А. В. (1961). Mathematical tables for research workers in human genetics, J and A Churchill, London.

781. McArthur N. (1953). Statistics in twin birth in Italy, 1949 and 1950, Ann. Eugen, 17, 249.

782. McClintock B. (1944). The relation of homozygous deficiencies to mutations and allelic series in Maize, Genetics, 29, 478-502.

783. McDevitt H. O. et al. (1972). Genetic control of the immune response, mapping of the Ir-1 locus, J. Exp. Med., 135, 1259-1278.

784. McKusick V.A. (1984). The human gene map 15 november 1983. The morbid anatomy of the human genome, Clin. Genet, 25, 89-123.

785. McMichael A., McDewitt H. (1977). The association between the HLA system and disease, ProG. Med. Genet. (New Series), 2, 39-100.

786. Menzel H.-J., Kladetzky R.-G., Assmann G. (1983). Apolipoprotein E polymorphism and coronary artery disease, Arteriosclerosis, 3, 310-315.

787. MetnekiJ., Czeizel A. (1980). Contraceptive pills and twins, Acta Genet. Med. Gemellol., 29, 233-236.

788. Migeon B. R., Miller S. С (1968). Humanmouse somatic cell hybrids with single human chromosome (group E): Link with thymidine kinase activity, Science, 162, 1005-1006.

7S9.Miki C., Yee S., Yasuda N., Morton N. E. (1969). Alltype. In: Morton N. E. (ed.), A genetic program library, The Univ. of Hawaii Press, Honolulu.

790. Milch R. A. (1959). A preliminary note of 47 cases of alcaptonuria occurring in 7 interrelated Dominican families, with an additional comment on two previously reported pedigrees, Acta Genet. (Basel), 9, 123-126.

791. Mohr J. (1954). A study of linkage in man. Opera ex Domo Biologiae Hereditariae Humanae Universitatis 33, Munksgaard, Copenhagen.

792. Mohr O. L., Wridt С (1919). A new type of hereditary brachyphalangy in man, Carnegie Inst. (Wash.), Publ, Nr. 295, 1-64.

793. Moll P. P. (1982). Alternative genetic models: An application to epilepsy. In: Anderson V. E. et al. (eds.), Genetic basis of the epilepsies, Raven Press, New York, pp. 277-289.

794. Moll P. P., Berry T. D., Weidman W. H., Ellefson R., GordsonH., Kottke B. A. (1984). Detection of genetic heterogeneity among pedigrees through complex segregation analysis: An application to hypercholesterolemia, Amer J. Hum. Genet., 36, 197-211.

795. Morch E. T. (1941). Chondrodystrophy dwarfs in Denmark, Opera ex Domo Biologiae Hereditariae Humanae Universitatis Hafniensis 3, Munksgaard, Copenhagen.

796. Morton N. E. (1956). The detection and estimation of linkage between the genes for elliptocytosis and the Rh blood type, Am. J. Hum. Genet., 8, 80-96.

797. Morton N. E. (1957). Further scoring types in sequential tests, with a critical review of autosomal and partial sex linkage in man, Am. J. Hum. Genet, 9, 55-75.

798. Morton N. E. (1955). Sequential tests for the detection of linkage, Am. J. Hum. Genet., 7, 277-318.

799. Morton N. E. (1962). Segregation and linkage. In: Burdette W. J. (ed.), Methodology in human genetics, Holden Day, San Francisco, pp. 17-52.

800. Morton N. E. (1969). Segregation analysis. In: Morton N. E. (ed.), Computer application in genetics, Univ. of Hawaii press, Honolulu, pp. 129-139.

801. Morton N. E. (1976). Genetic markers in atherosclerosis: a review, J. Med. Genet., 13, 81-90.

802. Morton N. E. (1983). Outline of genetic epidemiology, S. Karger, Basel etc.

803. Morton N. E., MacLean C. J. (1974). Analysis of family resemblance III, Complex segregation of quantitative traits, Am. J. Hum. Genet., 26, 489-503.

804. Morton N. E., Yee S., Elston R. C., Lew R. (1970). Discontinuity and quasi-continuity: Alternative hypothesesof multifactorial inheritance, Clin. Genet., 1, 81-93.

805. Morton N. E., Simpson S. P., Lew R., Yee S. (1983). Estimation of haplotype frequencies. Tissue Antigens, 22, 257-262.

806. Motulsky A. G. (1976). The genetic hyperlipidemias, N. Engl. J. Med., 294, 823-827.

807. Motulsky A. G. (1977). The George M. Kober lecture. A genetical view of modern medicine, Trans Assoc. Am. Physicians., 40, 76-90.

808. Motulsky A. G. (1978). The genetics of common diseases. In: Morton N. E., Chung C. S. (eds.), Genetic epidemiology, Academic Press, New York, pp. 541-548.

809. Motulsky A. G. (1979). The HLA complex and disease. Some interpretations and new data in cardiomyopathy, N. Engl. J. Med., 300, 918- 919.

810. Motulsky A. G. (1982). Genetic approaches to common diseases. In: Bonne-Tamir B. (ed.), Human Genetics, Part B, Medical Aspects, A Alan R. Liss, New York, pp. 89-95.

811. Motulsky A. G. (1980). Approaches to the genetics of common diseases. In: Rotter J. I., Samloff I. M., Rimoin D. L. (eds.), The Genetics and Heterogeneity of Common Gastrointestinal Disorders, Academic Press, New York, pp. 3-10.

812. Motulsky A. G. (1984). Editorial: Genetic epidemiology, Gen Epidemiol, 1, 143-144.

813. Motulsky A. G. (1984). Genetic research in coronary heart disease. In: Rao D. C., Elston R. C., Kuller L. N., Feinleib M., Carter C., Havlik R. (eds.), Genetic Epidemiology of Coronary Heart Disease, Pasr, Present, and Future, Alan R. Liss, New York, pp. 541-548.

814. Motulsky A. G. (1984). The "new genetics" in blood and cardiovascular research: applications to prevention and treatment, Circulation 70 (Suppl. Ill), III-26-III-30.

815. Motulsky A. G., Boman H. (1975). Genetics and atherosclerosis. In: Schettler G, Weizel A. (eds.), Atherosclerosis, Vol. Ill, Springer, Berlin, pp. 438-444.

816. Motulsky A. G., Boman H. (1975). Screening for the hyperlipidemias. In: Milunsky A. (ed.), The prevention of genetic disease and metal retardation, Saunders, Philadelphia, pp. 306-316.

817. Muhlmann W. E. (1930). Ein ungewohnlicher Stammbaum iiber Taubstummheit, Arch. Rassenbiol, 22, 181-183.

818. Munro A., Waldmann H. (1978). The major histocompatibility system and the immune response, Br.Med.Bull., 34, 253-258.

819. Murphy E. A. (1980). The quantitative genetics of disease, Am. J. Med. Genet, 7, 103-113.

820. Murphy E. A. (1981). The genetic dynamics of disease, Am. J. Med. Genet., 8, 35-52.

821. Murphy E. A. (1981). Only authorized persons admitted: The quantitative genetics of health and disease, Johns Hopkins Med. J., 148, 114-122.

822. Murphy E. A. (1982). Muddling, meddling, and modelinG. In: Anderson V. E. et al. (eds.), Genetic basis of the epilepsies, Raven Press, New York, pp. 333-348.

823. Nichtsheim H. (1950). The Pelger anomaly in man and rabbit. A Mendelian character of the nuclei leucocytes, J. Hered., 41, 131-137.

824. Naeslund J. (1956). Metodiken rid den forsta lasundervisningen. Enoversikt och experimen-tella bidrag, Svenska, Uppsala.

825. Nance W. E., McConnell F. E. (1973). Status and prospects of research in hereditary deafness, Adv. Hum. Genet, 4, 173-250.

825a.Nathans J., Piantanida T. P., Eddy R. L., Shows Т. В., HognessD.S. (1986). Molecular genetics of inherited variation in human color vision, Science, 232, 203-210.

826. Neel J. V., Fajons S. S., Conn J. W., Davidson К. Т. (1965). Diabetes mellitus. In: Neel J. V., Shaw M. W., Schull W. J. (eds.), Genetics and the epidemiology of chronic disease, Govt. Print. Office, Washington, pp. 105-132.

827. Neufeld H. N., GoldbourtU. (1983). Coronary heart disease: genetic aspects, Circulation, 67, 943.

828. Nicholas J. M., Jenkins W. J., Marsh W. L. (1957). Human blood chimeras. A study of surviving twins, Br. Med. J., 1, 1458.

829. Nora J. J. (1980). Identifying the child at risk coronary heart disease as an adult: a strategy for prevention, J. Pediatr., 97, 706-714.

830. Nora J. J., Lortscher R. H., Spongier R. D., Nora A. H., Kimberling W. J. (1980). Genetic-epidemiologic study of early-onset ischemic heart disease, Circulation, 62, 503-508.

831. Olefsky J. M. (1985). Diabetes mellitus. In: Wyngaarden J. В., Smith L. H. Jr. (eds.), Cecil Textbook of Medicine, 17th ed., WB Saunders, Philadelphia, pp. 1320-1341.

831a. Off J. (1974). Estimation of the recombination fraction in human pedifrees: Efficient computation of the likelihood for human linkage studies, Am. J. Hum. Genet., 26, 588-597.

831b. Off J. (1976). A computer program for linkage analysis general human pedigree, Am. J. Hum. Genet., 28, 528-529.

831c. Ott J. (1977). Counting methods (Em algorithm) in human pedigree analysis. Linkage and segregation analysis, Am. Hum. Genet., 40, 443-454.

832. Pauli R. M. (1983). Editorial comment: Dominance and homozygosity in man, Amer J. Med. Genet., 16, 455-458.

833. Pearson K. (1904). On the generalized theory of alternative inheritance with special referenses to Mendel's law, Philos. Trans. R. Soc. A, 203, 53-86.

834. Pearson R. J. С (1964). Blood groups and disease, Br. Med. J., I, 840.

835. Penrose R. J. С (1938). (Colchester survey). A clinical and genetic study of 1280 cases of mental defect, HMSO, London, Spec. Rep. Ser. Med. Res. CounC., 229.

836. Penrose L. S. (1947/49). The problem of anticipation in pedigrees of dystrophia myotonica, Ann. Eugen, 14, 125-132.

837. Penrose L. S. (1953). The genetical background of common disease, Acta Genet. (Basel), 4, 257-265.

838. Petranyi G. G., Irangi P., HolldnS.P. (1974). Relations of HL-A and Rh systems to immune reactivity, Vox. SanG., 27, 470-482.

839. Pious D., Erlich H., Gladstone P., Levine F. (1983). Analysis of the HLA region using somatic cell mutants. In: Caskey С. Т., White R. L. (eds.), Banbury Report 14, Cold Spring Harbor Laboratory, pp. 61-68.

840. Pola V., Svojitka J. (1957). Klassische Hamophilie bei Frauen, Folia Haematol. (Leipz.), 75, 43-51.

841. Poll H. (1914). Uber Zwillingsforschung als Hilfsmittel menschlicher Erbkunde, Z. Ethnol, 46, 87-108.

842. Propping P., Kruger J. (1976). Uber die Haufigkeit von Zwillingsgeburten, Dtsch. Med. Wochenschr., 101, 506-512.

843. Propping P., Vogel F. (1976). Twin studies in medical genetics, Acta Genet. Med. Gemellol (Roma), 25, 249-258.

844. Propping P., Voigtlander V. (1983). Was ist gesichert in der Genetik der Atopien? Allergologie, 6, 160-168.

845. Puska P., Tuomilehto J., Salonen J. et al. (1979). Changes in coronary risk factors during a comprehensive five-year community programme to control cardiovascular diseases (North Karelia Project), Br. Med. J., 2, 1173-1178.

846. Race R. R., Sanger R. (1969). Xg and sex chromosome abnormalities, Br. Med. Bull., 25, 99-103.

847. Rao C. D., Elston R. C., Kuller L. H., Feinleib M., Carter C., Havlik R. (eds.), (1984). Genetic Epidemiology of Coronary Heart Disease, Past, Present, and Future, Anan. R. Liss, New York.

848. Rappold G., Cremer Т., Cremer C., Back W., Bogenberger J., Cooke H. J. (1984). Chromosome assignment of two cloned DNA probes hybridizing predominantly to human sex chromosomes, Hum. Genet., 65, 257-261.

849. Rath B. (1938). Rotgrunblindheit in der Calmbacher Blutersippe. Nachweis des Faktorena-ustausches beim Menschen, Arch. Rassenbiol., 32 397-407.

850. Reed т. е., Neel J. V. (1959). Huntington's chorea in Michigan. 2. Selection and mutation, Am. J. Hum.Genet, 11, 107.

851. Rees A., Shoulders С. С, Stocks J., Galton D.J., Baralle F.E. (1983). DNA polymorphism adjacent to human apoprotein A-I gene: relation to hypertriglyceridemia, Lancet, 1, 444-446.

852. Reich Т., Rice J., Cloninger С. R., Wette R., James J. (1979). The use of multiple thresholds and segregation analysis in analyzing the phenotype heterogeniety of multifactorial traits, Ann. Hum. Genet., 42, 371-388.

853. Reid D. H., Parsons P. H. (1963). Sex of parents and variation of recombination with age in the mouse, Heredity, 18, 107.

854. Renwick J. H. (1956/7). Nailpatella syndrome: Evidence for modification by alleles at the main locus, Ann. Hum. Genet., 21, 159-169.

855. Renwick J. H. (1969). Progress in mapping human autosomes, Br. Med. Bull., 25, 65.

856. Richter S. (1967). Zur Hereditat des Strabismus concomitans, Humangenetik, 3, 235-243.

857. Richter S. (1966). Untersuchungen uber die Hereditat des Strabismus concomitans, Sammlung zwangloser Abhandlungen auf dem Gebiet der Augenheilkunde, Thieme, LeipziG.

857a.Robbins D. C., Blix P. M., Rubenstein A. H., Kanazawa Y., Kosaka K., Tager H. S. (1981). A human proinsulin variant at arginine 65, Nature, 291, 679-681.

858. Robertson F. W. (1981). The genetic component in coronary heart disease - review, Genet. Res. Camb., 37, 1-16.

859. Rose N. R., Vladutiu A. O., David С S., Shreffler D. C. (1973). Autoimmune murine thyroiditis. V. Genetic influence on the disease in BSVS and BRVR mice, Clin. Exp. Immunol., 15, (2), 281-287.

860. Rosenfield R. E., Allen F. H., Rubinstein P. (1973). Genetic model for the Rh blood group system, Proc. Natl. Acad. Sci. USA, 70, 1303 1307.

861. Rotter J. I., Rimoin D. L. (1981). The genetics of the glucose intolerance disorders, Am. J. Med., 79, 116-126.

862. Rudiger H. W., Dreyer M. (1983). Pathogenetic mechanisms of hereditary diabetes mellitus, Hum. Genet., 63, 100-106.

863. Rushton W. A. H. (1975). Visual pigments and color blindness, Sci. Am., 232(3), 64-75.

864. Scott J., Knott T. J., Priestley L. M., Robertson M.E., Mann D. V., Kostner G., Miller G. J., Miller N. E. (1985). Highdensity lipoprotein composition is altered by a common DNA polymorphism adjacent to apoprotein All gene in man, Lancet, 1, 771-773.

865. Selby P. B., SelbyP.R. (1978). Gammaray-induced dominant mutations that cause skeletal abnormalities in mice. II. Description of proved mutations, Mutat. Res., 51, 199-236.

866. Sheppard P. M. (1975). Natural selection an heredity, 4th ed., Hutchinson, London.

867. Shoelson S., Haneda M., Blix P., Nanjo A., Sanke T., Inouye K., Steiner D., Rubenstein A., Tager H. (1983). Three mutant insulins in man, Nature, 302, 540-543.

868. Shows Т. В., Sakagychi A. Y., Nay lor S. L. (1982). Mapping the human genome, cloned genes, DNA polymorphism and inherited disease, Adv. Hum. Genet., 12, 341-452.

869. Siemens H. W. (1924). Die Zwillingspathologie, Springer, Berlin.

870. Siemens H. W. (1924). Die Leistungsfahigkeit derzwillingspathologischen Arbeitsmethode, Z. Induktive Abstammungs-Vererbungslehre, 33, 348.

871. Siemens H. W. (1925). Ober einen, in der menschlichen Pathologie noch nicht beobachten Vererbungsmodus: Dominant geschlechtsgebundene Vererbung, Arch. Rassenbiol., 17, 47-61.

872. Simon M., Alexandre J. L., Bourel M., Le Marec В., Scordia C. (1977). Heredity of idiopathic haemochromatosis: a study of 106 families, Clin. Genet., 11, 327-241.

872a. Simon M., Bourel M., Genetet В., Fauchet R. (1977). Idiopathic hemochromatosis: demonstration of recessive transmission and early detection by family HLA typing, N. Engl. J. Med., 297, 1017-1021.

873. Simonds B. (1963). Tuberculosis in twins, Putnam, London.

874. Sing С. F., Davignon J. (1985). Role of the apolipoprotein E polymorphism in determining normal plasma lipid and lipoprotein variation, Am. J. Hum. Genet, 37,

875. Slack J. (1979). Inheritance of familial hypercholesterolemia. In: Paoletti R., Grott A. M. Jr. (eds.), Atherosclerosis Reviews, Vol. 5, Raven Press, New York, pp. 35-66.

875a. Smith Ch. (1971). Recurrence risks for multifactorial inheritance. Am. J. Hum. Genet., 23, 578-588.

876. Smith С. А. В. (1956). A test for segregation ratios in family data, Ann. Hum. Genet., 20, 257.

877. Smith С. А. В. (1956/7). Counting methods in genetical statistics, Ann. Hum. Genet., 21, 254-276.

878. Smith C. A. B. (1959). A note on the effect of ascertainment on segregation ratios, Ann. Hum. Genet., 23, 311-323.

879. Smith C. A. B. (1970). A note on testing the Hardy-Weinberg law, Ann. Hum. Genet., 33, 377.

880. Smith C. H. (1970). Heritability of liability and concordance in monozygous twins, Ann. Hum. Genet., 34, 85.

881. Smith S. M., Penrose L. S. (1955). Monozygotic and dizygotic twin diagnosis, Ann. Hum. Genet., 19, 273-289.

882. Smith S. M., Penrose L. S., Smith C. A. B. (1961). Mathematical tables for research workers in human genetics, Churchill, London.

883. Smithies O. (1964). Chromosomal rearrangements and protein structure, Cold Spring Harbor Symp. Quant. Biol., 29, 309.

884. Smithies O., Connell G. E., Dixon G. H. (1962). Chromosomal rearrangements and the evolution of haptoglobin genes, Nature, 196, 232.

885. Snyder L. F., Doan С. A. (1944). Is the homozygous form of multiple teleangiectasia lethal? Lab. Clin. Med, 29. 1211-1216.

886. Sorensen H., Dissing J. (1975a). Association between the C3F gene and atherosclerotic vascular diseases, Hum. Hered, 25, 279-283.

887. Southern E. M. (1982). Application of DNA analysis to mapping the human genome, Cytogenet. Cell Genet., 32, 52 57.

888. Svejgaard A., Jersild C., Staub Nielsen L., Bodmer W. F. (1974). HL-A antigens and disease. Statistical and genetical considerations, Tissue Antigens, 4, 95-105.

889. Svejgaard A., Hauge M., Jersild C., Platz P., Ryder L. P., Staub Nielsen L., Thomsen M. (1979). The HLA system. An introductory survey, 2nd ed, Karger, Basel, New York.

890. Swanson J., Park В., McCullough J. (1972). Kell phenotypes in families of patients with X-linked chronic granulomatous disease, 12th Congress of the International Society for Blood Transfusion, Washington (Abstracts), p. 26.

891. Schaefer E. J. (1984). Clinical, biochemical, and genetic features in familial disorders of high density lipoprotein deficiency, Arteriosclerosis, 4, 303-322.

892. Schepank H. (1974). Erb- und Umweltfactoren bei Neurosen, Psychiatry Series, 11, 1-221.

893. Schiff F., v Verschuer O. (1933). Serologische Untersuchungen an Zwillingen. II. Mitt. Z. Morphol. Anthropol., 32, 244-249.

894. Schnyder U. W. (1955). Neirodermitis und Allergie des Respirationstraktes, Dermatologica, 110, 289.

895. Schroeder T.-M., Tilgen D., Kruger J., Vogel F. (1976). Formal genetics of Fanconi's anemia, Hum.Genet., 32, 257-288.

895a. Schrott H. G., Karp L., Omenn G. S. (1973). Prenatal prediction in myotonic dystrophy: guidelines for genetic counseling, Clin. Genet, 4, 38-45.

896. Steinberg A. G. (1965). Evidence for a mutation or crossing over at the Rhlocus, Vox Sang, 10, 721.

897. Stern С (1957). The problem of complete Y-lihkage in man, Am. J. Hum. Genet., 9, 147-165.

898. Stern C., Walls G. L. (1957). The Cunier pedigree of "color blindness", Am. J. Hum. Genet., 9, 249-273.

899. Stevenson A. C., Cheeseman E. A. (1955/56). Hereditary deaf mutism with particular reference to Northern Ireland, Ann. Hum. Genet., 20, 177-231.

900. Stevens W. L. (1950). Statistical analysis of the ABO blood groups, Hum. Biol., 22, 191-217.

901. Stocks P., Barrington A. (1925). Hereditary disorders of bone development, Treasury of Human Inheritance 3, Part I.

902. Stone N. J. (1979). Genetic hyperdipidemia and atherosclerosis, Artery, 5, 377-397.

903. Strasser G. (1982). Coronary risk factors revisited, World Health Forum, 3, 85-88.

904. Sturtevant A. H. (1925). The effect of unequal crossing over at the bar locus in drosophila, Genetics, 10, 117.

%4a.Svejgaard A., Platz P., Ryder L. P. (1983). HLA and disease 1982. In: Moller G. (ed.), HLA and disease susceptibility (Immunological reviews, vol. 70), Munksgaard, Copenhagen, pp. 193-218.

905. Tatter sail R. (1976). The inheritance of maturityonset type diabetes in young people. In: Creutzfeldt E., Kobberling J., Neel J. V. (eds.), The genetics of diabetes mellitus, Springer Verlag, Berlin, Heidelberg, New York, pp. 88-95.

906. Tattersall R. В., Руке D. A. (1972). Diabetes in identical twins, Lancet, II, 1120-1125.

907. ten Kate L. P., Boman H., Daiger S. P., Motulsky A. G. (1982). Familial aggregation of coronary heart disease and its relation to known genetic risk factors, Am. J. Cardiol., 50, 945-953. 908. ten Kate L. P., Boman H., Daiger S. P., Motulsky A. G, (1984). Increased frequency of coronary heart disease in relatives of wives of myocardial infarct survivors: assortative mating for lifestyle and risk factors, Am. J. Cardiol., 53, 399-403.

910. Terasaki P. I. (1980). Histocompatibility testing 1980, UCLA Tissue Typing Laboratory, Los Angeles.

911. Terasaki P. I., McClelland J. D. (1964). Microdroplet assay of human serum cytotoxins, Nature, 204, 998-1000.

912. Timofeef-Ressovsky N. W. (1931). Gerichtetes Variieren in der Phanotypischen Manifestierung einiger Generationen von Drosophila funebris, Naturwissenschaften, 19, 493-497.

913. TolleshaunG. H., Goldstein J. L., Schneider W. J., Brown M. S. (1982). Posttranslational processing of the LDL receptor and ist genetic disruption in familial hypercholesterolemia, Cell, 30, 715-724.

914. Trevor-Roper P. D. (1952). Marriage of two complete albinos with normally pigmented offspring, Br. J. Ophthalmol., 36, 107.

915. Utermann G. (1983). Coronary heart disease. In: Emery A.E.H., Rimoin D. L. (eds.), Principles and practice of medical genetics, Churchill Livingstone, Edinburgh etc., pp. 956-978.

916. Utermann G., Hardewig A., Zimmer F. (1984). Apolipoprotein E phenotypes in patients with myocardial infarction, Hum. Genet., 65, 237-241.

917. Utermann G., Kindermann I., Kaffarnik H., Steinmetz A. (1984). Apolipoprotein E phenotypes and hyperlipidemia, Hum. Genet., 65, 232-236.

918. Verschuer O. von (1954). Wirksame Faktoren im Leben des Menschen, Steiner, Wiesbaden.

919. Verschuer O. von (1958). Die Zwillingsforschung im Dienste der inneren Medizin, Verh. Dtsch. Ges. Inn. Med., 64, 262-273.

920. Vogel F. (1969). Does the human X chromosome show evidence for clustering of genes with related functions? J. Genet. Hum., 17, 475-477.

921. Vogel F. (1970). The genetic basis of the normal human electroencephalogram (EEG), Hum. Genet, 10, 91-114.

922. Vogel F. (1957). Methoden zur Prufung der Reihenfolge von Merkmalstragern und Gesunden in Geschwisterschaften, Z. Menschl. Vererbungs-Konstitutionslehre, 34, 194-204.

923. Vogel F. (1982). Die Bedeutung der Humangenetik fur eine Theorie der Krankheit, Verh. Dtsch. Ges. Path., 66, 1-15.

924. Vogel F., Dorn H. (1964). Erbliche Hautkrankheiten, In: Becker P. E. (ed.), Humangenetik, ein kurzes Handbuch, Vol. IV, Thieme, Stuttgart, pp. 346-535.

925. Vogel F., Kruger J. (1967). Multifactorial determination of genetic affections, Proceedings of the 3rd International Congress of Human Genetics, Johns Hopkins University Press, Baltimore, pp. 437-445.

926. Vogel F., Wendt G. G. (1956). Zwillingsuntersuchung uber die Erblichkeit einiger ahthropologischer Masse und Konstituonsindices, Z. Menschl. Vererbungs-Konstitutionslehre, 33, 425-446.

927. Waardenburg P. J. (1957). The twin study method in wider perspective, Acta Genet. (Basel), 7, 10-20.

928. Waarneburg P. J. (1953). Zum Kapitel des ausserokularen erblichen Nystagmus, Acta Genet. (Basel), 4, 298-312.

929. Wahlund S. (1928). Zusammensetzung von Populationen und Korrelationserscheinungen vom Standpunkt der Vererbungslehre aus betrachtet, Hereditas, 11, 65-105.

930. Walter H. (1976). Kdrperbauform und Klima. Kritische Uberlegungen zur Obertragbarkeit der Bergmann'schen Regel auf den Menschen, Z. Morphol. Anthropol., 67, 241-263.

931. Watkins Winifred M. (1966). Blood-group substances, Science, 152, 172-181.

932. Weicker H. (1959). Die genetischen Grundlagen der Fanconi-Anamie, Schweiz. Med. Wochenschr., 89, 1081.

933. Weight M., Cortese C., Sule U., Miller N. E., Lewis B. (1982). Heritability of the low density lipoprotein receptor activity of human blood mononuclear cells: studies in normolipidaemic adult male twins, Clin. Sci., 62, 397-401.

934. Weinberg W. (1902). Beitrage zur Physiologie und Pathologie der Mehrhngsgeburten beim Menschen und Probleme der Mehrlingsgebur tenstatistik, Z. Geburtshilfe Gynakol., 47, 12.

935. Weinberg W. (1909). Der Einfluss von Alter und Geburtenzahl der Mutter auf die Haufigkeit der ein- und zweieiigen Zwillingsgeburten, Z. Geburtshilfe Gynakol., 65, 318-324.

936. Weinberg W. (1912). Methoden und Fehlerquel-len der Untersuchung auf Mendelsche Zahlen beim Menschen, Arch. Rassenbiol., 9, 165-174.

937. Weiner W., Lewis H. В. М., Moores P., Sanger R., Race R. R. (1957). A gene, y, modifying the blood group antigen A, Vox SanG., 2, 25-37.

938. Weiss M. C., Green H. (1967). Humanmouse hybrid cell lines containing partial complements of human chromosomes and functioning human genes, Proc. Natl. Acad. Sci. USA, 58, 1104-1111.

939. Weitkamp L. R. (1972). Human autosomal linkage groups. Proceedings of the 4th International Congress of Human Genetics, Paris, 1971, Excerpta Medica, Amsterdam, pp. 445-460.

940. Welander L. (1957). Homozygous appearance of distal myopathy, Acta Genet. (Basel), 7, 321-325.

941. Wendt G. G., Drohm D. (1972). Fortschritte der Allgemeinen und Klinischen Humangenetik, Vol. IV, Die Huntingtonsche Chorea, Thieme, Stuttgart.

942. Werdelin O. (1982). Immune response genes, Allergy, 37, 451-461.

943. Wettke-Schafer R., Kantner G. (1983). X-linked dominant inherited diseases with lethality in hemizygous males, Hum. Genet., 64, 1-23.

944. White R., Leppert M., Bishop D. Т., Barker D., I Berkowitz J., Brown C., Callahan P., Holm Т., Jerominski L. (1985). Construction of linkage J maps with DNA markers for human chromosomes, Nature, 313, 101-105.

945. White R. (1985). Mapping human chromosomes I in genetic diseases. First Intrn. Symp. on the I Role of Recombinant DNA in Genetics (Teplitz R. L. et al., eds.), Crete (In the press, 1986).

946. White R., Leppard M., Bishop D. Т., Barker D., Berkowitz J., Brown C., Callahan R., Holm Т., Jerominski L. (1985). Constitution of linkage maps with DNA markers for human chromosomes, Nature, 313, 101-105.

947. Whittingham S., Mathews J. D., Schanfield M. S., Tait B. D., Mackay I. R. (1981). Interaction of HLA and Gm in autoimmune chronic active hepatitis, Clin. Exp. Immunol., 43, 80-86.

948. Wieland W. (1975). Diagnose. Uberlegungen zur Medizintheorie, De Gruyter, Berlin, New York.

949. Wieland W. (1983). Systematische Bemerkungen zum Diagnosebegriff, Munstersche Beitrage zur Geschichte und Theorie der Medizin, 20, 17-34.

950. Wiener A. S. (1943). Additional variants of the Rh type demonstable with a special human anti-Rh-serum, J. Immunol., 47, 461-465.

951. Wiener A. S. (1941). Hemolytic reactions following transfusion of blood of the homologous group II, Arch. Pathol., 32, 227-250.

952. Wiener A. S., di Diego N., Sokol S. (1953). Studies on the heredity of the human blood groups, I. The MN type, Acta Genet. Med. Gemellol. (Rome), 2, 391-398.

953. Williams D. L. (1985). Molecular biology in arteriosclerosis research. Arteriosclerosis, 5, 213-227.

954. Williams W. R., Lalouel J. M. (1982). Complex segregation analysis of hyperlipidemia in a Seattle sample, Hum. Hered., 32, 24-26.

955. Wilson S. R. (1973). The correlation between relatives under the multifactorial model with assortative mating I. The multifactorial model with assortative mating I. The multifactorial model with assortative matting, Ann. Hum. Genet., 37, 189-204.

956. Wilson S. R. (1973). The correlation between relatives under the multifactorial model with assortative matinG. II. The correlation between relatives in the equilibrium position, Ann. Hum. Genet., 37, 205-215.

957. Wimer В. М., Marsh W. L., Taswell H. F., Galey W. R. (1977). Haemological changes associated with the McLeod phenotype of the Kell blood group system, Br. J. Haematol, 36, 219.

958. Winters R. W., Graham J. В., Williams Т. F., McFalls V. C., Burnett С. Н. (1957). A genetic study of familial hypophosphatemia and vitamin D-resistant rickets, Trans. Assoc. Am. Physicians., 70, 234-242.

959. Woolf B. (1955). On estimating the relation between blood group and disease, Ann. Hum. Genet, 19, 251-253.

960. Wright S. (1934). The results of crosses between inbred strains of guinea pigs differing in number of digits, Genetics, 19, 537-551.

961. Wright S. (1931). Evolution in Mendelian populations, Genetics, 16, 97-159.

962. Yasuda N., Tsuji K. (1975). A counting method of maximum likelihood for estimating haplotype frequency in the HL-A system, Jap. J. Hum. Genet., 20, 1.

963. Yee S., Lew R., Morton N. E. (1969). A general program for segregation analysis. In: Morton N. E. (ed.), A. genetics program Library, The Univ. of Hawaii Press, Honolulu.

964. Yokoyama S. (1985). DNA polymorphism and the susceptibility to diabetes, Am. J. Med. Genet, 21, 649-654.