References

Anonymous. (1997a). Molecular medicine: A primer for clinicians. Part X: Clinical implications of the new genetics—I. South Dakota Journal of Medicine, 50(11), 401-404.

Anonymous. (1997b). Molecular medicine: A primer for clinicians Part XI: Clinical implications of the new genetics—II. South Dakota Journal ofMedicine, 50(12), 445-448.

Atran, S. (1998). Folk biology and the anthropology of science: Cognitive universals and cultural particulars. Behavior and Brain Sciences, 21(4), 547-569; discussion 569-609.

Bajema, C. J. (Ed.). (1971). Natural selection in human populations. New York: Wiley.

Boyce, A. J. et al. (1976). Association between PTC-taster status and goitre in a Papuan New Guinea population. Human Biology, 48(4), 769-773.

Bratosiewicz, J., Liberski, P. P. et al. (2001). Codon 129 polymorphism of the PRNP gene in normal Polish population and in Creutzfeldt-Jakob disease, and the search for new mutations in PRNP gene. Acta Neurobiologiae Experimentalis (Warsz), 61(3), 151-156.

Carr, D. H., & Gedeon, M. (1977). Population cytogenetics of human abortuses. In E. B. Hook & I. H. Porter (Eds.), Population cytogenetics: Studies in humans (pp. 1-10). New York: Academic Press.

Cavalli-Sforza, L. L., Menozzi, P., & Piazza, A. (1994). The history and geography of human genes. Princeton, NJ: Princeton University Press.

Childs, B., Moxon, E. R., & Winkelstein J. A. (1992). 5. Genetics and infectious diseases. In R. A. King, J. I. Rotter, & A. G. Morulsky (Eds.), The genetic basis of common diseases (pp. 71-91). New York & Oxford, UK: Oxford University Press.

Collins, F. S., & Gelehrter, T. D. (1992). 2. Molecular genetics. In R. A. King, J. I. Rotter, & A. G. Morulsky (Eds.), The genetic basis ofcommon diseases (pp. 19-33). New York & Oxford, UK: Oxford University Press.

Darwin, C. (1868). The variation of animals and plants under domestication. London: John Murray.

Dunn, L. C. (1965). A short history of genetics: The development of some of the main lines of thought, 1864-1939. Ames: Iowa State University Press.

Gajdusek, D. C., & Zigas, V. (1957). Degenerative disease of the central nervous system in New Guinea: The epidemic occurrence of "kuru" in the native populations. New England Journal of Medicine, 257, 974-978.

Glass, B. (1968). Maupertuis, pioneer of genetics and evolution. In B. Glass, O. Temkin, & W. L. Straus, Jr. (Eds.), Forerunners of Darwin, 1745-1859 (pp. 51-83). Baltimore: Johns Hopkins University Press.

Habener, J. F., & Williams, G. W. (2001). The metabolic basis of common inherited diseases. Philadelphia: W. B. Saunders.

Haig, D. (2000). Genomic imprinting, sex-biased dispersal, and social behavior. Annals of the New York Academy of Sciences, 907, 149-163.

Joner, G., & Sovik, O. (1989). Increasing incidence of diabetes mellitus in Norwegian children 0-14 years of age 1973-1982. Diabetologia, 32(2), 79-83.

King, R. A., Rotter, J. I., & Morulsky, A. G. (1992). 1. The approach to genetic bases of common diseases. In R. A. King, J. I. Rotter, & A. G. Morulsky (Eds.), The genetic basis of common diseases (pp. 3-18). New York & Oxford, UK: Oxford University Press.

Konotey-Ahulu, F. I. D. (1991). The sickle cell disease patient. Houndsmills, UK: Macmillan.

Lenz, F. (1931). Morbid hereditary factors. In E. Bauer, E. Fischer, & F. Lenz (Eds.), Human heredity (pp. 213-492). New York: Macmillan.

Leridon, H. (1977). Human fertility. Chicago: University of Chicago Press.

Levy-Marchal, C. (1998). Evolution of the incidence of IDDM in childhood in France. Revue Epidemiologie Sante Publique, 46(3), 157-163.

Lewis, R. (2001). Human genetics (4th ed.). Boston: McGraw-Hill.

Mai, L. L., Young Owl, M., & Kersting. P. (2004). Dictionary of human biology and evolution. Cambridge, UK: Cambridge University Press.

Mange, E. J., & Mange, A. P. (1999). Basic human genetics (2nd ed.). Sunderland, MA: Sinauer.

Marks, J. (2001). Scientific and folk ideas about heredity. In R. A. Zilinskas & P. J. Balint, (Eds.), The human genome project and minority communities: Ethical, social and political dilemmas (pp. 53-66). Westport, CO: Praeger.

Matthews, J. D. et al. (1968). Kuru and cannibalism. The Lancet, 2(7565), 449-452.

McElroy, A., & Townsend, P. K. (1996). Medical anthropology in ecological perspective (3rd ed.). Boulder, CO: Westview Press.

McKee, L. (1987). Ethnomedical treatment of children's diarrheal illnesses in the highlands of Ecuador. Social Science & Medicine, 25(10), 1147-1155.

Mittwoch, U. (1986). Males, females, and hermaphrodites. Annals of Human Genetics, 50, 103-121.

Nesse, R. M., & Williams, G. C. (1996). Darwinian medicine. New York: Random House.

North, A. F., Jr., Gorwitz, K. et al. (1977). A secular increase in the incidence of juvenile diabetes mellitus. Journal of Pediatrics, 91(5), 706-710.

Nzewi, E. (2001). Malevolent ogbanje: Recurrent reincarnation or sickle cell disease? Social Science & Medicine, 52(9), 1403-1416.

Onwubalili, J. K. (1983). Sickle cell anaemia and reincarnation beliefs in Nigeria. The Lancet, 2(8364), 1423.

Pool, R. (1992). Wrestling anticancer secrets from garlic and soy sauce. Science, 257(5075), 1349.

Prusiner, S. B., & Scott, M. R. (1997). Genetics of prions. Annual Review of Genetics, 31, 139-175.

Rhodes, R. (1997). Deadly feasts: The "prion" controversy and the public's health. New York: Touchstone/Simon & Schuster.

Richards, M. (1997). It runs in the family: Lay knowledge about inheritance. In A. Clarke & E. Parsons (Eds.), Culture, kinship and genes: Towards cross-cultural genetics (pp. 175-194). New York: St. Martin's Press.

Russell, N. (1986). Like engendering like: Heredity and animal breeding in early modern England. Cambridge, UK: Cambridge University Press.

Scriver, C. R., Beaudet, A. L., Sly, W. S., & Valle,D. (Eds.). (1995). The metabolic and molecular basis of inherited disease (7th ed.). New York: McGraw-Hill.

Stearns, S. C. (Ed.). (1999). Evolution in health and disease. New York: Oxford University Press.

Terleph, T. A. (2000). Resisting biology. The unpopularity of a gene's-eye view. Annuals of the New York Academy of Sciences, 907, 212-217.

Trevathan, W., McKenna, J. L., & Smith, E. O. (Eds.). (1999).

Evolutionary medicine. New York: Oxford University Press. Vogel, F., & Motulsky, A. G. (1999). Human genetics: Problems and approaches (3rd ed.). New York: Springer-Verlag. Will, R. G., Zeidler, M. et al. (2000). Diagnosis of new variant Creutzfeldt-Jakob disease. Annals of Neurology, 47(5), 575-582. Windl, O., Dempster, M. et al. (1996). Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: A systematic analysis of predisposing mutations and allelic variation in the PRNP gene. Human Genetics, 98(3), 259-264.

Zilinskas, R. A., & Balint, P. J. (Eds.). (2001). The human genome project and minority communities: Ethical, social and political dilemmas. Westport, CO: Praeger.

Zimmerman, K., Turecek, P. L. et al. (1999). Genotyping of the prion protein gene at codon 129. Acta Neuropathologica (Berlin), 97(4), 355-358.

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