Литература к главе 6

1713. Adams M. S., Neel J. V. (1967). Children of incest, Pediatrics, 40, 55-62.

1714. Allison A. C. (1954). Protection afforded by sicklecell trait against subtertian malaria infection, Br. Med. J., I, 290.

1715. Allison A. C. (1954). The distribution of the sicklecell trait in East Africa and elsewhere, and its apparent relationship to the incidence of subtertian malaria, Trans. R. Soc. Trop. Med. HyG., 48, 312.

1716. Allison A. C. (1954). Notes on sicklecell polymorphism, Ann. Hum. Genet., 19, 39.

1717. Allison A. C. (1955). Aspects of polymorphism in man, Cold Spring Harbor Symp. Quant. Biol., 20, 239.

1718. Allison A. C. (1956). The sickle and hemoglobin C-genes in some African populations, Ann. Hum. Genet, 21, 678.

1719. Allison A. C. (1964). Polymorphism and natural selection in human populations, Cold Spring Harbor Symp. Quant Biol., 24, 137-149.

1720. Anonymous (1983). WHO Working Group (including A Motulsky and 13 others): Community control of hereditary anaemias, Bull. WHO, 61, 63-80. Also published in French, Bull. WHO, 61, 277-297.

1721. Antonarakis S. E., Boehm C. D., Serjeant G. R., Theisen C. E., Dover G. J., Kazazian H. H. (1984). Origin of the figlobin gene in Blacks: The contribution of recurrent mutation or gene conversion or both, Proc. Natl. Acad. Sci. USA, 81, 853-856.

1722. Baird P. A., McGillivray B. (1982). Children of incest, J. Pediatr., 101, 854-857.

1723. Bashi J. (1977). Effects of inbreeding on cognitive performance, Nature, 266, 440-442.

1724. Beet E. A. (1946). Sicklecell disease in the Balovale district of North Rhodesia, East Afr. Med. J., 23, 75.

1725. Beet E. A. (1947). Sicklecell disease in Northern Rhodesia, East Afr. Med. J., 24, 212-222.

1726. Bergeron P., Laberge C., Grenier A. (1974). Hereditary tyrosinemia in the province of Quebec: Prevalence at birth and geographic distribution, Clinical Genetics, 5, 157-162.

1727. Bernhard W. (1966). Uber die Beziehung zwischen ABO-Blutgruppen und Pockenster-blichkeit in Indien und Pakistan, Homo, 17, 111.

1728. Block J. (1901). Der Ursprung der Syphilis, Fischer, Jena.

1729. Blumberg B. S., Hesser J. E. (1971). Loci differently affected by selection in two American black populations, Proc. Natl. Acad. Sci. USA, 68, 2554.

1730. Bois E., Feingold J., Demenais F., Runavot Y., Jehanne M., Toidic L (1978). Cluster of cystic fibrosis cases in a limited area of Brittany (France), Clin. Genet., 14. 73-76.

1731. Bosnjakovic S. (1938). Vererbungsverhaltnise bei der sogenannten Krankheit von Mljet, Acta Derm. Venereol. (Stockh.), 19, 88.

1732. Brues A. M. (1954). Selection and polymorphism in the ABO blood groups, Am. J. Phys. Anthropol., 12, 559-598.

1733. Cann R. L., Brown W. M., Wilson A. C. (1984). Polymorphic sites and the mechanism of evolution in human mitochondrial DNA, Genetics, 106, 479-499.

1734. Carter C. O. (1967). Risk of offspring of incest, Lancet, I, 436.

1735. Cavalli-Sforza L. L., Edwards A. W. F. (1967). Phylogenetic analysis: Models and estimations procedures, Evolution, 21, 550-570.

1736. Cerimele D., Cottoni F., Scappaticci S., Rabbiosi G., Sanna E., Zei G., Fraccaro M. (1982). High prevalence of Werner's syndrome in Sardinia. Description of six patients and estimate of the gene frequency, Hum. Genet., 62, 25-30.

1737. Chakravartti M. R., Vogel F. (1971). Haemaglutinatior-inhibiting variola antibodies in blood serum of former smallpox-patients, their healthy siblings and unvaccinated controls in other areas, Humangenetik, 11, 336-338.

1738. Charnov E. (1977). An elementary treatment of kin selection, J. Theor. Biol., 66, 541-550.

1739. Clarke B. (1975). Frequency-dependent and density-dependent natural selection. In: The role of natural selection in human evolution, Salzano F. (ed.), North Holland, American Elsevier, Amsterdam, New York, pp. 187-200.

1740. Clarke L. A. (1974). Rh haemolytic disease, Original papers commentaries, Medical and Technical Publ. Сотр., Newcastle.

1741. Comings D. E. (1982). Twodimensional gel electrophoresis of human brain proteins. III. Genetic and non-genetic variations in 145 brains, Clin. Chem., 28, 798-804.

1742. Cooper D. N., Smith B. A., Cooke H. J., Niemann S., Schmidtke J. (1985). An estimate of unique DNA sequence heterozygosity in the human genome, Hum. Genet., 69, 201-205.

1743. Costeff H., Cohen B. E., Weller L., Rahman D. (1977). Consanguinity analysis in Israeli mental retardates, Am. J. Hum. Genet., 29, 339-349.

1744. Crabb A. R. (1947). The hybridcorn makers, New Brunswick.

1745. Crow J. F. (1958). Some possibilities for measuring selection intensities in man, Hum. Biol., 30, 1-13.

1746. Crow J. F. (1963). 2. The concept of genetic load: A reply, Am. J. Hum. Genet., 15, 310-315.

1747. Crow J. F. (1970). Genetic loads and cost of natural selection. In: Mathematical topics in population genetics, Kojima K. (ed.), Springer, Berlin, Heidelberg, New York, pp. 128- 177.

1748. Crow J. F., Denniston С (1981). The mutation component of genetic damage, Science, 212, 888-893.

1749. Cruz-Coke R. (1982). Nomogram for estimating specific consanguinity risk, J. Med. Genet., 19, 216-217.

1750. Dahlberg G. (1929). Inbreeding in man, Genetics, 14, 421-454.

1751. Damian R. T. (1964). Molecular mimicry: antigen sharing by parasite and host and its concequences, Am. Naturalist, 98, 129-150.

1752. Das B. M., Chakravartti M.R., Delbruck H., Flatz G. (1971). High prevalence of Haemoglobin E in two populations in Assam, Hum. Genet., 12, 264-266.

1753. Das B. M., Deka R. (1975). Predominance of the haemoglobin E gene in a Mongoloid population in Assam (India), Hum. Genet., 30, 187-191.

1754. Dobzhansky T. (1952). Nature and origin of heterosis. In: Heterosis, Gowen J. W. (ed.), Iowa State College Press, p. 218.

1755. Downie H. W., Meiklejohn G., Vincent L. St., Rao A. R., Sundara Babu B.V., KempeC.H. (1966). Smallpox frequency and severity in relation to А, В and О blood groups, Bull. WHO, 33, 623.

1755a. East E. M., Jones D. F. (1919). Inbreeding and outbreeding, Lippincot. London, Philadelphia.

1756. Eichner E. R., Finn R., KrevansJ.R. (1963). Relationship between serum antibody levels and the ABO blood group polymorphism, Nature, 198, 164.

1757. Ewens W. J. (1980). Mathematical population genetics, Springer, Berlin, Heidelberg, New York.

1758. Firschein I. L (1961). Population dynamics of the sickle cell trait in the Black Caribs of British Honduras, Am. J. Hum. Genet, 13, 233.

1759. Fisher R. A. (1930). The distribution of gene ratios for rare mutations, Proc. R. Soc. Edinb., 50, 205-220.

1760. Flatz G. (1967). Haemoglobin E: Distribution and population dynamics, Hum. Genet, 3, 189-234.

1761. Flatz G. (1976). Populationsgenetik der Hamoglobinanomalien, Humangenetik, ein kurzes Handbuch, Becker P. E. (ed.), Vol. III/3, Thieme, Stuttgart, pp.557-579.

1762. Flatz G., Pik C., Sundharayati B. (1964). Malaria and haemoglobin E in Thailand, Lancet, П, 385.

1762a. Flatz G., Oelbe M., Herrmann H. (1983). Ethnic distribution of phenylketonuria in the North German population, Hum. Genet., 65, 396-399.

1763. Fraser G. R., Mayo O. (1974). Genetic load in man (Review), Hum. Genet, 23, 83-110.

1764. Freire-Maia N., Azevedo J. B. C. (1971). The inbreeding load in Brazilian White and Negro populations as estimated with sib and cousin controls, Am. J. Hum. Genet, 23, 1-7.

1765. Freire-Maia N. et al. (1983). Inbreeding studies in Brasilian schoolchildren, Am. J. Med. Genet, 16, 331-355.

1766. Friedman M. J., Trager W. (1981). The biochemistry of resistance to malaria, Sci. Am., 244, 154-164.

1767. v. Fumetti C. (1976). Inzuchtkoeffizienten und Haufigkeiten konsanguiner Ehen., BioloG. Di-plomarbeit, HeidelberG.

1768. Georges A., Jacquard A. (1968). Effects de la consanguinite sur la montalite infantile. Results d'une observation dans le departement des Vosges, Population, 23, 1055-1064.

1769. Giblett E. R. (1977). Genetic polymorphisms in human blood, Ann. Rev. Genet, 11, 13-28.

1770. Glass R. I., Holmgren J., Haley С. Е., Khan M.R., Svennerholm A.-M., Stoll B.J., Hossain К. М. В., Black R. E., Yunus M., Barua D. (1985). Predisposition for cholera of individuals with 0 blood group, Am. J. Epidemiol., 121, 791-796.

1771. Goodman R. M., Motulsky A. G. (eds.) (1979). Genetic diseases among Ashkenazi Jews, Raven Press, New York.

1772. Greiner J., Schleiermacher E., Smith Т., lenhard V., Vogel F. (1978). The HLA system and leprosy in Thailand, Hum. Genet, 42, 201-213.

1773. Greenberg L. J., Gray E. D., Yunis E. J. (1975). Association of HL-A5 and immune responsiveness in vitro to streptococcal antigens, J. Exp. Med., 141, 935-943.

1774. Grove D. I., Forbes I. J. (1975). Increased resistance to helminth infestation in an atopic population, Med. J. Australia, 1, 336-338.

1775. Haldane J. B. S. (1937). The effect of variation on fitness, Am. Naturalist, 71, 337-349.

1776. Haldane J. B. S. (1939). The spread of harmful autosomal recessive genes in human populations, Ann. Eugen, 9, 232-237.

1777. Haldane J. B. S. (1942). Selection against hete-rozygotes in man, Ann. Eugen, 11, 333.

1778. Haldane J. B. S. (1949). The rate of mutations of human genes. Proceedings of the 7th International Congress on Genetics, Hereditas [Suppl.], 35, 267.

1779. Haldane J. B. S. (1955). On the biochemistry of heterosis, and the stabilization of polymorphism, Proc. R. Soc. (London) [Biol], 144, 217-220.

1780. Haldane J. B. S. (1957). The cost of natural selection, J. Genet, 55, 511-524.

1781. Haldane J. B. S., Moshinsky P. (1939). Inbreeding in Mendelian populations with special reference to human cousin marriage, Ann. Eugen, 9, 321-340.

1782. Hamaguchi H., Yamada M., Shibasaki M., Mukai R., Yabe Т., Kondo I. (1982). Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis: 3. Frequent occurrence of genetic variants in some abundant polypeptides of PHA-stimulated peripheral blood lymphocytes, Hum. Genet., 62, 142-147.

1783. Hamaguchi H., Ohta A., Mukai R., Yabe Т., Yamada M. (1981). Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis. I. Detection of genetic variant proteins in PHA-stimulated peripheral blood lymphocytes, Hum. Genet., 59, 215-220.

1784. Hamilton W. D. (1964). The genetical evolution of social behavior. I. J. Theoret. Biol., 7, 1-16.

1785. Hanhart E. (1955). Zur mendelistischen Auswertung einer 33 Jahre langen Erforschung von Isolaten. Navant'Anni dell Leggi Mendeliane, Ed. Orrizante Medico, Roma, pp. 397 415.

1786. Harris R., Harrison G. A., Rondle C.J.M. (1963). Vaccinia virus and human blood group A substance, Acta Genet, (Basel), 13, 44.

1787. Harris H., Hopkinson D. A. (1972). Average heterozygosity per locus in man: an estimate based on the incidence of enzyme polymorphisms, Ann. Hum. Genet., 36, 9-20.

1788. Harris H., Hopkinson A., Robson E. B. (1974). The incidence of rare alleles determining elec-trophoretic variants: Data on 43 enzyme loci in man, Ann. Hum. Genet, 37, 237-253.

1789. Helmbold W. (1959). Uber den Zusammenhang zwischen ABO-Blutgruppen und Krankheit Betrachtungen zur Ursache der ABO-Fre-quenzverschiebung bei Patienten mit Carcinoma ventriculi, carcinoma genitalis und ulcus pepticum, Blut, 5, 7-22.

1790. Hiernaux J. (1952). La genetique de la sickle-mie et l'interet anthropologique de sa frequence en Afrique noir, Annal Mus. Congo Beige, Science de 1'homme, Anthropologie, 2, Tervuren, 42 pp.

1790a. Hill A. V. S., Wainscoat J. S. (1986). The evolution of the a and P-Globin gene clusters in human populations, Hum. Genet., (in the press).

1791. Hirsch A. (1981). Handbuch der historisch-geographischen Pathologie, Part 1, Infektions-krankheiten, 2nd ed., Enke, Stuttgart.

1792. Horai S., Gojobori Т., Matsunaga E. (1984). Mitochondrial DNA polymorphism in Japanese, Hum. Genet, 68, 324-332.

1793. Ifediba T. C., Stern A., Ibrahim A., Rieder R. F. (1985). Plasmodium falciparum in vitro: diminished growth in hemoglobin H disease erythrocytes, Blood, 65, 452-455.

1794. lshikumi N., Nemoto H., Neel J. V., Drew A. L., Yanase Т., Matsumoto YS. (1960). Hosojima, Am. J. Hum. Genet., 12, 67-75.

1795. Jeffreys A. J., Wilson K., Theim S. L. (1985). Hypervariable "minisatellite" regions in human DNA, Nature, 314, 67-73.

1796. Jeffreys A. J., Wilson V., Theim S.L. (1985). Individual-specific 'fingerprints' of human DNA, Nature, 316, 76-79.

1797. Jonxis J. H. P. (1959). The frequency of haemoglobin S and С carriers in Curacao and Surinam, Symposium on Abnormal Hemoglobins, Blackwell, Oxford.

1798. Kellermann G. (1972). Further studies on the ABO typing of ancient bones, Hum. Genet., 14, 232-236.

1799. Kidson C., Lament G., Saul A., Nurse G. T. (1981). Ovalocytic erythrocytes from Melanesians are resistant to invasion by malaria parasites in culture, Proc. Natl. Acad. Sci. USA, 78, 5829-5832.

1800. Kircher W. (1961). Untersuchungen uber den Zusammenhang von Dyspepsieverlauf und ABO-Blutgruppenzugehorigkeit, Monatsschr. Kinderheilkd., 109, 369.

1801. Kircher W. (1964). Weitere Untersuchungen uber den Zusammenhang zwischen Verlauf und Haufigkeit deo Sauglingsenteritis and ABO - Blutgruppenzugehorigkeit, Monatsschr. Kinderheilkd., 112, 415.

1802. Klinger K. W. (1983). Cystic fibrosis in the Ohio Amish: Gene frequency and founder effect, Hum. Genet., 65, 94-98.

1803. Klose J., Willers L., Singh S., Goedde H. W. (1983). Twodimensional electrophoresis of soluble and structurebound proteins from cultured human fibroblasts and hair root cells: Qualitative and quantitative variation, Hum. Genet, 63, 262-267.

1804. Krieger H., Vicente A. T. (1969). Smallpox and the ABO system in Southern Brazil., Hum. Hered., 19, 654.

1805. Lambotte-Legrand J., Lambotte-Legrand C. (1955). Anemie drepanocytaire et homozygo-tisme (a propos de 300 cas.), Ann. Soc. Beige Med, Trop., 35, 47.

1806. Levy H. L. (1973). Genetic screening, Adv. Hum. Genet, 4, 1-104.

1807. Lewontin R. C. (1967). An estimate of average heterozygosity in man, Am. J. Hum. Genet, 19, 681-685.

1808. Lewontin R. C. (1977). Population genetics, Proceedings of the 5th International Congress on Human Genetics 1976, Armendares S, Lisker R. (eds.), Excerpta Medica, Amsterdam, Oxford, pp. 13-18.

1809. Li С. С. (1963). 3. The way the load works, Am. J. Hum. Genet, 15, 316-321.

1810. Li C. C. (1976). First course in population genetics, Boxwood, Pacific Grove. [Имеется перевод: Ли, Введение в популяционную генетику.-М.: Мир, 1978.]

1811. Livingstone F. B. (1957). Sickling and malaria, Brit. Med. J, I, 762.

1812. Livingstone F. B. (1958). Anthropological implications of sickle cell gene distributions in West Africa, Am. Anthropologist, 60, 533-562.

1813. Livingstone F.B. (1962). The origin of the sickle cell gene. Conference on African Historical Anthropology, Northwestern University, Chicago.

1814. Livingstone F. B. (1971). Malaria and human polymorphism, Ann. Rev. Genet, 5, 33-64.

1815. Livingstone F. B. (1973). Data on the abnormal hemoglobins and glucose-6-phosphate dehydrogenase deficiency in human populations, 1967-1973, University of Michigan, Ann. Arbor.

1815a. Livingstone F. B. (1985). Frequencies of Hemoglobin Variants. Thalassemia, The Glucose 6-Phosphate Dehydrogenase Deficiency, G6PD Variants, and Ovalocytosis in Human Populations, Oxford, New York.

1816. Livingstone F. B. (1983). The malaria hypothesis. In: Distribution and Evolution of Hemoglobin and Globin Loci, Bowman J. E. (ed.), Elsevier, New York, pp. 15-44.

1817. Uvingstone F. B. (1984). The Duffy blood groups, vivax malaria, and malaria selection in human populations: a review, Hum. Biol, 56, 413-425.

1818. London W. T., Sutnick A. I., Millman I., Coyne V., Blumberg B. S., Vierucci A. (1972). Australia antigen and hepatitis: Recent observations on the serum protein polymorphism, infectious agents hypothesis, Canad. Med. Ass. J, 106, Special Issue, 480-485.

1819. Ludwig W. (1944). Uber Inzucht und Verwandtschaft, Z. Menschl. Vererbungs Konstitutionslehre, 28, 278-312.

1820. Lundborg H. (1913). Medizinisch - biologische Familienforschungen innerhalb eines 2232-kopfigen Bauerngeschlechtes in Schweden (Provinz Blekinge). 2 vols, Fischer, Jena.

1821. Luzzatto L. (1979). Genetics of red cells and susceptibility to malaria, Blood, 54, 961.

1822. Luzzatto L., Sodeinde O., Martini G. (1983). Genetic variation in the host and adaptive phenomena in Plasmodium falciparum infection. In: Malaria and the Red Cell, Evered D, Whelan J. (eds.) Pittman, London, pp. 159-173.

1823. Luzzatto L., UsangaE.A., Reddy S. (1969). Glucose-6-phosphate dehydrogenase deficient red cells resistance to infection by malarial parasites, Science, 164, 839.

1824. Majewski F. (1980). Untersuchungen zur Al-koholembryopathie, Thieme Verlag, Stuttgart.

1825. McKusick V. A., Egeland J. A., Eldridge R., Krusen D. R. (1964). Dwarfism in the Amish I. The Ellisvan Creveld syndrome, Bull. Johns Hopkins Hosp, 115, 306.

1826. Morton N. E. (1955). Nonrandomness in consanguineous marriage, Ann. Hum. Genet, 20, 116-124.

1827. Morton N. E., Crow J. F., Muller H. J. (1956). An estimate of the mutational damage in man from data on consanguineous marriages, Proc. Natl. Acad. Sci. USA, 42, 855-863.

1828. Morton N. E., Matsuura J., Bart R., Lew R. (1978). Genetic epidemiology of an institutionalized cohort of mental retardates, Clin. Genet, 13, 449-461.

1829. Motulsky A. G. (1984). Hereditary red cell traits and malaria, Am. J. Trop. Med. HyG., 13(1), Part 2, 147-158.

1830. Motulsky A. G. (1975). Glucose-6-phosphate dehydrogenase and abnormal hemoglobin polymorphisms-evidence regarding malarial selection. In: The role of natural selection in human evolution, Salzano F. (ed.), North-Holland, Amsterdam, pp. 271-291.

1831. Motulsky A. G. (1960). Metabolic polymorphism and the role of infectious disease in human evolution, Hum. Biol., 32, 28-62.

1832. Motulsky A. G. (1979). Possible selective effects of urbanization on Ashkenazi Jewish population. In: Genetic Diseases Among Ashkenazi Jews, Goodman R. M., Motulsky A. G. (eds.), Raven Press 1979, New York, pp. 201-212.

1833. Motulsky A. G. (1980). Ashkenazi Jewish gene pools: admixture, drift and selection. In: Population Structure and Genetic Disorders, Eriksson A. W., Forsius H., Nevanlinna H. R., Workman P. L., Norio R. K. (eds.), Academic Press, London, pp. 353-365.

1834. Motulsky A. G., Murray J. С (1983). Conference summary: current concepts of gemoglobin genetics. In: Distribution and Evolution of Hemoglobin and Globin Loci, Bowman J. E. (ed.), Elsevier, New York, pp. 345-355.

1835. Muller H. J. (1950). Our load of mutation, Am. J. Hum. Genet., 2, 111-176.

1836. Neel J. V. (1951). The population genetics of two inherited blood byscrasias in man, Cold Spring Harbor Symp. Quant. Biol., 15, 141.

1837. Nell J. V. (1979). History and the Tay-Sachs allele. In: Goodman R.M., Motulsky A. G. (eds.), Genetic diseases among Ashkenazi Jews, Raven Press, New York, pp. 285-299.

1838. Nel U. V., Rosenblum B. B., Sing C.F., Skolnick M.M., Hanash S.M., Sternberg S. (1984). Adapting two-dimensional gel electrophoresis to the study of human germline mutation rates. In: Two dimensional gel electrophoresis of proteins, Academic Press, New York, pp. 259-306.

1839. Nell J. V., Schull W.J. (1962). The effect of inbreeding on mortality and morbidity in two Japanese cities, Proc. Natl. Acad. Sci. USA, 48, 573.

1840. Neel. J. V., Schull W.J., Kimura Т., Yanijawa Y, Yamamoto M., Nakajima A. (1970). The effect of parental consanguinity and inbreeding in Hirado, Japan. III. Vision and hearing, Hum. Hered., 20, 129-155.

1841. Nei M., Li W. H. (1979). Mathematical model for studying genetic variation in terms of restriction endonucleases, Proc. Natl. Acad. Sci, USA, 76, 5269-5273.

1842. Norio R., Nevalinna H. R., Perheentupa J. (1973). Hereditary diseases in Finland: Rare flora in rare soil, Ann. Clin. Res., 5, 109-141.

1843. Often C. M. (1967). On pestilence, diet, natural selection, and the distribution of microbial and human blood group antigens and antibodies, Curr. Anthropol., 8, 209.

1844. Pasval G., Weatherall D. J., Wilson J. M. (1978). Cellular mechanism for the protective effect of haemoglobin S against falciparum malaria, Nature, 274, 701-703.

1845. Pasvol G. (1982). The interaction of malaria parasites with red blood cells, Br. Med. Bull., 38, 133-140.

1846. Pasvol G., Wainscoat J. S., Weatherall D. J. (1982). Erythrocytes deficient in glycophorin resist invasion by the malarial parasite Plasmodium falciparum, Nature, 297, 64.

1847. Pasvol G., Weatherall D. J., Wilson R. J. M. (1978). Cellular mechanism for the protective effect of haemoglobin S against P. falciparum malaria, Nature, 274, 701-703.

1847a. Pasvol G., Weatherall D. J., Wilson R. J. M. (1977). Effect of foetal haemoglobin on susceptibility of red cells to Plasmodium falciparum, Nature, 270, 171-173.

1848. Penrose L. S., Smith S. M., Sprott D. A. (1956). On the stability of allelic systems, with special reference to haemoglobin A, S, and C., Ann. Hum. Genet., 21, 90-93.

1849. Pettenkofer H. J., Bickerich R. (1960). Uber Antigen-Gemeinschaften zwischen den menschlichen Blutgruppen und gemeingefahrli-chen Krankheiten, Zentralbl. Bakteriol., I, Abt. 179.

1850. Pettenkofer H. J., Stoss В., Helmbold W., Vogel F. (1962). Alleged causes of the presentday world distribution of the human ABO blood groups, Nature, 193, 444.

1851. Phills J. A., Harrold J., Whiteman G. V., Perelmutter L. (1972). Pulmonary infiltrates, asthma and eosinophilia due to Ascaris suum infestation in man, New Engl. J. Med., 286, 965-970.

1852. Piazza A. et al. (1973). In: Histocompatibility Testing 1972 (Report of an International Workshop and Conference held at Evian, 23-27 may 1972), Dausset J., Colombani J. (eds.), Munksgaard, Copenhagen, pp. 73-84.

1853. Povey S., Hopkinson D. A. (1981). The use of polymorphic enzyme markers of human blood cells in genetics, Clin. Haematol., 10, 161-184.

1854. Rao P. S. S., Inboraj S. G. (1979). Trends in human reproductive wastage in relation to longterm practice of inbreeding, Ann. Hum. Genet. 42 401-413.

1855. Rao P. S. S., Inboraj S. G. (1980). Inbreeding effects on fetal growth and development, J. of Med. Genet., 17, 27-33.

1856. Reed S. C. (1954). A test for heterozygous deleterious recessives, J. Hered., 45, 17-18.

1857. Reed Т. Е. (1969). Caucasian genes in American negroes, Science, 165, 762-768.

1858. Robinson M. G., Tolchin D., Halpern С (1971). Enteric bacterial agents and the ABO blood groups, Am. J. Hum. Genet., 23, 135.

1859. Roth E. F. Jr., Raventos-Suarez C., Rinaldi A., Nagel R. L (1983). Glucose-6-phosphate dehydrogenase deficiency inhibits in vitro growth of Plasmodium falciparum, Proc. Natl. Acad. Sci. USA, 80, 298.

1860. Roth E. F. Jr., Raventos-Suarez C., Rinaldi A., Nagel R. L. (1983). The effect of X chromosome inactivation on the inhibition of Plasmodium falciparum malaria growth by glucoses-phosphate dehydrogenase - deficient red cells, Blood, 62, 866.

1861. Roth E. Jr., Raventos-Suarez C., Gilbert H., Stump D., Tanowitz H., Rowin K.S., Nagel R. L. (1984). Oxidative stress and falciparum malaria: a critical review of the evidence. In: Malaria and the Red Cell, Alan R. Liss, New York, pp. 35-43.

1862. Salzano F.M. (ed.) (1975). The role of natural selection in human evolution, North Holland, Amsterdam, Oxford.

1863. Sanghvi L.D. (1963). The concept of genetic load: A critique, Am. J. Hum. Genet., 15, 298-309.

1864. Sanghvi L.D., Balakrishnan V. (1972). Comparison of different measures of genetic distance between human populations. In: The assessment of population affinities in man, Weiner J. S., Huisinga (eds.), Clarendon, Oxford, pp. 25-36.

1865. Sangvichien S. (1966). A preliminary report on nonmetrical characteristics of neolithic skeletons found at Bankhoro, Kanchanaburi, J. Siam. Soc. (Bangkok), 54, 1.

1866. Sasazuki Т., Kohno Y, Iwamoto I., Tanimura M., Naito S. (1978). Association between an HLA haplotype and low responsiveness to tetanus toxoid in man, Nature, 272, 359-361.

1867. Seemanova E. (1971). A study of children of incestuous matings, Hum. Hered., 21, 108-128

1868. Shull G. H. (1908). Composition of a field of maize, Rep. Am. Breeders AssoC., 4, 296-301.

1869. Shull G. H. (1911). Experiments with maize, Bot. Gaz., 52, 480.

1870. Sjogren T. (1931). Die juvenile amaurotische Idiotie, Hereditas, 14, 197-425.

1871. Slatis H. M. (1954). A method of estimating the frequency of abnormal autosomal recessive genes in man, Am. J. Hum. Genet., 6, 412- 418.

1872. Smith S.M. (1954). Notes on sickle-cell polymorphism, Ann. Hum. Genet., 19, 51.

1873. Socha W, Bilinska M., Kaczera Z., Pajdak E., Stankiewicz D. (1969). Escherichia coli and ABO blood groups, Folia Biol. (Krakow), 17, (4).

1874. Sukamaran P.K., Master H.R., Unde-sia J. V., Balakrishnan В., Sanghvi L.D. (1966). ABO blood groups in active cases of smallpox, Indian J. Med. Sci., 20, 119.

1875. Sussmilch (1786). Die gottliche Ordnung, 9th ed., Teil II, Berlin.

1876. Schull W.J. (1958). Empirical risks in consanguineous marriages: Sex ratio, malformation, and viability, Am. J. Hum. Genet., 10, 294-343.

1877. Schull W.J., Furusho Т., Yamamoto M. et al. (1970). The effects of parental consanguinity and inbreeding in Hirado, Japan. IV. Fertility and reproductive compensation, Hum. Genet., 9, 294-315.

1878. Schull W.J., Nagano H, Yamamoto M.,

Komatsu I. (1970). The effect of parental consanguinity and inbreeding in Hirado, Japan. I. Stillbirth and prereproductive mortality, Am. J. Hum. Genet., 22, 239-262.

1879. Schull W.J., Nell J.V. (1972). The effect of parental consanguinity and inbreeding in Hirado, Japan. V. Summary and interpretation, Am. J. Hum. Genet., 24, 425-453.

1880. Tanis R. J., Neel J.V., Dovey H., Morrow M. (1973). The genetic structure of a tribal population, the Yamomama Indians. IX. Gene frequencies for 17 serum protein and erythrocyte enzyme systems in the Yamomama and five neighboring tribes; nine new variants, Am. J. Hum. Genet., 25, 655-676.

1881. Thalhammer O. (1975). Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world. A collaborative study, Hum. Genet, 30, 273-286.

1882. Vandepitte J. M., Zuelzer W. W., Neel J. V., Colaert J. (1955). Evidence concerning the inadequacy of mutation as an explanation of the frequency of the sickle-cell gene in the Belgian Congo, Blood, 10, 341.

1883. de Vries R. R. P., Fat R. F. M. L. A., Nijenhuis L. E., van Rood J. J. (1976). HLA-linked genetic control of host response to mycobacterium leprae, Lancet, II, 1328-1330.

1884. de Vries R.R.P., van Rood J.J. (1977). Abstract Tissue Antigens, 10, 212.

1885. Vogel F. (1970). Anthropological implications of the relationship between ABO blood groups and infections, Proceedings of the 8th International Congress of Anthropologic and Ethnologic Sciences, Tokyo, 1968, Vol. I, p. 365.

1886. Vogel F. (1979). 'Our load of mutation': reappraisal of an old problem, Proc. Roy. Soc., London, В 205, 77-90.

1887. Vogel F. (1979). Genetics of retinoblastoma, Hum. Genet., 52, 1-54.

1888. Vogel F., Chakravartti M.R. (1966). ABO blood groups and smallpox in a rural population of West Bengal and Bihar (India), Hum. Genet, 3, 166-180.

1889. Vogel F., Dehnert J., Helmbold W. (1964). Uber Beziehungen zwischen ABO-Blutgruppen und der Sauglingsdyspepsie, Hum. Genet, 1, 31-57.

1890. Vogel F.. Pettenkofer H. J., Helmbold W. (1960). Uber die Populationsgenetik der ABO - Blutengruppen. II. Genhaufigkeit und epidemiche Erkrankungen, Acta Genet. (Basel), 10, 267-294.

1891. Wade Cohen P. Т., Omenn G. S., Motulsky A. G., Chen S.-H, Giblett E.R. (1973). Restricted variation in the glycolytic enzymes of human brain and erythrocytes, Nature, 241, 229.

1892. Walton K. E., Steyer D., Gruenstein E. I. (1979). Genetic polymorphism in normal human fibroblasts as analyzed by two-dimensional polyacrylamide gel electrophoresis, J. Biol. Chem, 254, 7951-7960.

1893. Weiner J. S., Huizinga J. (ed.) (1972). The assessment of population affinities in man, Clarendon, Oxford.

1894. Workman P. L., Blumberg B. S., Cooper A. J. (1963). Selection, gene migration and polymorphic stability in U. S. White anj Negro population, Am. J. Hum. Genet., 15, 429.

1895. Wright S. (1922). Coefficients of inbreeding and relationshir, Am. Naturalist, 56, 330-338.

1896. Zerbin-Rudin E. (1960). Vorlaufiger Bericht uber den Gesundheitszustand von Kindern aus nahen Blutsverwandtenehen, Z. Menschl. Vererbungs-, Konstitutionslehre, 35, 233-302.

1897. Zuckerkandl E. (1976). Evolutionary processes and evolutionary noise at the molecular level, J. Mol. Evol., 7, 167-183.