Moments of truth in genetic medicine

Moments of Truth in Genetic Medicine

Volumn , Issue , 2005, Pages 1-270

  Lindee, M Susan ^a  

^a NONE

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EID: 84895125465     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Book

References (380)

1. Acosta, Phyllis. 1977. Diet management of PKU for infants and preschool children. Washington, DC: U. S. Department of Health, Education and Welfare, no. 77-5209.
2. Adams, Mark B. 1989a The politics of human heredity in the USSR, 1920-1940. Genome 31(2):879-884.
3. -. 1989b. The wellborn science: Eugenics in Germany, France, Brazil and Russia. Oxford: Oxford University Press.
4. Aguayo, A. J., C. P. Nair, and G. M. Bray. 1971. Peripheral nerve abnormalities in the Riley-Day syndrome: Findings in a sural nerve biopsy. Archives of Neurology 24:106-116.
5. Allen, Garland E. 2001. Is a new eugenics afoot? Science 294(5540):59-61.
6. Allen, Gordon. 1968. Diagnostic efficiency of fingerprint and blood group differences in a series of twins. Acta Geneticae Medicae et Gemellologiae 17(2):359-374.
7. Allen, Richard J. 1960. The detection and diagnosis of phenylketonuria. American Journal of Public Health 50(11):1662-1666.
8. Alliance of Genetic Support Groups. 1995. Directory of national genetic voluntary organizations. Chevy Chase, MD: The Alliance.
9. Allison, A. C. 1954. Protection afforded by sickle cell trait against subtertial malarial infection. British Medical Journal 1:290-294.
10. Aly, Gotz, Peter Chroust, and Christian Pross. 1994. Cleansing the fatherland: Nazi medicine and racial hygiene, trans. Belinda Cooper; foreword by Michael H. Kater. Baltimore: Johns Hopkins University Press.
11. American Society of Human Genetics. 1995. Report. American Journal of Human Genetics 57:1233-1241.
12. Anderson, John A., and Kenneth F. Swaiman. 1966. Phenylketonuria and allied metabolic diseases. Washington, DC: U. S. Children's Bureau.
13. Anderson, S. L., R. Coli, I. W. Daly, E. A. Kichula, M. J. Rork, S. A. Volpi, J. Ekstein, and B. Y. Rubin. 2001. Familial dysautonomia is caused by mutations of the IKAP gene. American Journal of Human Genetics 68(3):753-758.
14. Andrews, Lori B., Jane E. Fullarton, Neil A. Holtzman, and Arno G. Motulsky (Committee on Assessing Genetic Risks, Institute of Medicine), eds. 1994. Assessing genetic risks: Implications for health and social policy. Washington, DC: National Academy Press.
15. Armstrong, M. D., and F. H. Tyler. 1955. Studies on phenylketonuria: I. Restriction of phenylalanine intake in phenylketonuria. Journal of Clinical Investigation 34:565-580.
16. Arnstein, Shirley Young. 2000. No tears: Living with familial dysautonomia. Phoenix, AZ: Via Press.
17. Aronowitz, Robert. 1998. Making sense of illness: Science, society and disease. Cambridge: Cambridge University Press.
18. Axelrod, Felicia. 1997a. Familial dysautonomia: Manual of comprehensive care. New York: Dysautonomia Foundation.
19. -. 1997b. Familial dysautonomia. In Clinical autonomic disorders, ed. P. A. Low, 2nd ed., 525-535. Philadelphia: Lippincott-Raven.
20. Axelrod, Felicia, Hedi L. Leistner, and Robert Porges. 1974. Breech presentation among infants with familial dysautonomia. Journal of Pediatrics 84(1):107-109.
21. Barr, M. L., and E. G. Bertram. 1949. A morphological distinction between neurones of the male and female, and the behavior of the nucleolar satellite during accelerated nucleoprotein synthesis. Nature 163:676.
22. Bender, M. A., and M. A. Kastenbaum. 1969. Statistical analysis of the normal human karyotype. American Journal of Human Genetics 21(4):322-351.
23. Benirschke, K., Lydia Brownhill, D. Hoefnagel, and F. H. Allen Jr. 1962. Langdon Down anomaly (mongolism) with 21/21 translocation and Klinefelter's syndrome in the same sibship. Cytogenetics 1:75-89.
24. Bergen, A. A., A. S. Plomp, E. J. Schuurman, S. Terry, M. Breuning, H. Dauwerse, J. Swart, M. Kool, S. Van Soest, F. Baas, J. B. Ten Brink, and P. T. De Jong. 2000. Mutations in ABCC6 cause pseudoxanthoma elasticum. Nature Genetics 25(2):228-231.
25. Berkowitz, Edward D., and Mark J. Santangelo. 1999. The Medical Follow-Up Agency: The first fifty years, 1946-1996. Washington, DC: National Academy Press.
26. Bessman, S. P. 1968. PKU-some skepticism. New England Journal of Medicine 278(21):1176-1177.
27. Bessman, Samuel, and Judith Swazey. 1971. Phenylketonuria: A study of biomedical legislation. In Human aspects of biomedical innovation, ed. Everett Mendelsohn, Judith Swazey, and Irene Taviss, 49-76. Cambridge: Harvard University Press.
28. Bevis, D. C. A. 1952. The antenatal prediction of haemolytic disease of the newborn. Lancet 1:395-398.
29. Bickel, H. 1996. The first treatment of phenylketonuria. European Journal of Pediatrics 155(July, suppl. 1):S2-S3.
30. Bickel, H. Gerrard, and E. M. Hickmans. 1953. Influence of phenylalanine intake on phenylketonuria. Lancet 2:812-813.
31. Blum, K., E. P. Noble, P. J. Sheridan, A. Montgomery, T. Ritchie, P. Jagadeeswaran, H. Nogami, A. H. Briggs, and J. B. Cohn. 1990. Allelic association of human dopamine D receptor gene in alcoholism. Journal of the American Medical Association 263(15):2055-2060.
32. Blumenfeld, A., S. A. Slaugenhaupt, F. B. Axelrod, D. E. Lucente, C. Maayan, C. B. Liebert, L. J. Ozelius, J. A. Trofatter, J. L. Haines, X. O. Breakefield, et al. 1993. Localization of the gene for familial dysautonomia on chromosome 9 and definition of DNA markers for genetic diagnosis. Nature Genetics 4:160-164.
33. Breo, Dennis L. 1994. The cancer revolution-from black box to genetic disease. Journal of the American Medical Association 217(18):1452-1454.
34. Bridges, T. J., J. L. Pool, and C. M. Riley. 1949. Central autonomic dysfunction with defective lacrimation: II. Preliminary report of effect of neurosurgery in one case. Pediatrics 3(4):479-481.
35. Brumberg, Joan Jacobs. 1988. Fasting girls: The emergence of anorexia nervosa as a modern disease. Cambridge: Harvard University Press.
36. Brunt, P. W., and Victor A. McKusick. 1970. Familial dysautonomia: A report of genetic and clinical studies, with a review of the literature. Medicine 49(5):343-374.
37. Carey, John. 1994. The next wonder drug may not be a drug. Business Week, 9 May.
38. Carter-Saltzman, Louise, and Sandra Scarr. 1977. MZ or DZ? Only your blood grouping laboratory knows for sure. Behavior Genetics 7(4):273-280.
39. Caspersson, T., S. Farber, G. Foley, J. Kudynoski, E. Modest, E. Simonsson, U. Wagh, and L. Zech. 1968. Chemical differentiation along metaphase chromosomes. Experimental Cell Research 49(1):219-222.
40. Cattell, Jacques, ed. 1955. American men of science, 9th ed. Lancaster, PA: Science Press; New York: R. R. Bowker.
41. -. 1972. American men and women of science: Formerly American men of science; a biographical directory founded in 1906, 12th ed. Lancaster, PA: Science Press; New York: R. R. Bowker.
42. Cederlof R., L. Friberg, E. Jonsson, and L. Kaij. 1961. Studies on similarity diagnosis in twins with the aid of mailed questionnaires. Acta Genetica 11:338-362.
43. Centerwall, Willard, and Siegfried Centerwall. 1965. Phenylketonuria: An inherited metabolic disorder associated with mental retardation. Washington, DC: Children's Bureau, U. S. Department of Health, Education and Welfare.
44. Centerwall, Willard R., Robert F. Chinnock, and Albert Pusavat. 1960. Phenylketonuria: Screening programs and testing methods. American Journal of Public Health 50(11):1667-1677.
45. Chadwick, B. P., M. Leyne, S. Gill, C. B. Liebert, J. Mull, E. Mezey, C. M. Robbins, H. W. Pinkett, I. Makalowska, C. Maayan, A. Blumenfeld, F. B. Axelrod, M. Brownstein, J. F. Gusella, and S. A. Slaugenhaupt. 2000. Cloning, mapping and expression of a novel brain-specific transcript in the familial dysautonomia candidate region on chromosome 9q31. Mammalian Genome 11(1):81-83.
46. Chen, W J., H. W Chang, M. Z. Wu, C. C. Lin, C. Chang, Y. N. Chiu, W. T. Soong. 1999. Diagnosis of zygosity by questionnaire and polymarker polymerase chain reaction in young twins. Behavior Genetics 29(2):115-123.
47. Chicago Conference: Standardization in Human Cytogenetics. 1966. Report. Birth Defects Original Articles Series 2 (2).
48. Childs, Barton. 1970. Sir Archibald Garrod's conception of chemical individuality: A modern appreciation. New England Journal of Medicine 282(2):71-77.
49. -. 1999. Genetic medicine: A logic of disease. Baltimore: Johns Hopkins University Press.
50. Chu, Ernest H. Y. 1960a. The chromosome complements of human somatic cells. In Symposium on cytology and cell culture genetics of man, ed. Gordon Allen, 97-103. Bethesda, MD: National Institutes of Health.
51. -. 1960b. The chromosome complements of the human somatic cell. American Journal of Human Genetics 12(1):97-103.
52. Clark, T., and M. Hughes. 1992. Sickle cell mutual help groups: African Americans supporting one another. Chapel Hill: Psychological Research Division, University of North Carolina.
53. Clause, Bonnie Tocher. 1993. The Wistar rat as a right choice: Establishing mammalian standards and the ideal of a standardized mammal. Journal of the History of Biology 26:333.
54. Clayson, David, Wooster Welton, and Felicia Axelrod. 1980. Personality development and familial dysautonomia. Pediatrics 65(2):269-274.
55. Clifford, C. A., and J. L. Hopper. 1986. The Australian NHMRC Twin Registry: A source for the Australian scientific community. Medical Journal of Australia 145:63-65.
56. Cockburn, W C, B. Hobson, J. W. Lightbown, J. Lyng, and D. Magrath. 1992. The international contribution to the standardization of biological substances: III. Biological standardization and the World Health Organization 1947-1990. Biologicals 20(1):1-10.
57. Cohen, M. M., Margery Shaw, and Jean W. MacCluer. 1966. Racial difference in the length of the human Y chromosome. Cytogenetics 5:34-52.
58. Collins, Francis. 1998. Foreword. In Inherited susceptibility to cancer: Clinical, predictive and ethical perspectives, ed. William D. Foulkes and Shirley V. Hodgson. Cambridge: Cambridge University Press.
59. Committee for the Study of Inborn Errors of Metabolism. 1975. Genetic screening: Programs, principles and research. Washington, DC: National Academy of Sciences.
60. Comuzzi, A. G., and D. B. Allison. 1998. The search for human obesity genes. Science 280:1374-1377.
61. Cook-Deegan, Robert Mullan. 1995. Gene wars: Science, politics and the Human Genome Project. New York: W. W Norton.
62. Court Brown, W M., K. E. Buckton, P. A. Jacobs, I. M. Tought, E. V. Kuensberg, and J. D. E. Knox. 1966. Chromosome studies on adults, vol. 42 of Eugenics lab memoirs. London: Cambridge University Press.
63. Cowan, Ruth Schwartz. 1992. Genetic technology and reproductive choice: An ethics for autonomy. In The code of codes: Scientific and social issues in the Human Genome Project, 245-263. Cambridge: Harvard University Press.
64. Dancis, Joseph. 1973 The prenatal detection of hereditary defects. In Medical genetics, ed. Victor McKusick and Robert Claiborne. New York: H. P. Publishing.
65. -. 1983. Familial dysautonomia. In Autonomic failure: A textbook of clinical disorders of the autonomic nervous system, ed. Roger Bannister, 615-639. Oxford: Oxford University Press.
66. Daston, Lorraine, and Katherine Park. 1998. Wonders and the order of nature, 1150-1750. Cambridge, MA: Zone Books, MIT Press.
67. De Chadarevian, Soraya. 2002. Designs for life: Molecular biology after World War II. Cambridge: Cambridge University Press.
68. De Chadarevian, Soraya, and Harmke Kamminga, eds. 1998. Molecularizing biology and medicine: New practices and alliances, 1910s-1970s. Amsterdam: Harwood Academic.
69. De La Chapelle, Albert. 1961. Constrictions in normal human chromosomes. Lancet 26(Aug.):460-464.
70. Dell Aringa, Stefanie. 1997. Dr. Axelrod brings hope to patients with rare disease. American Academy of Pediatrics News 10 (5).
71. Denver Study Group. 1960a. A proposed standard nomenclature of human mitotic chromosomes. Lancet 1:1063-1065.
72. -. 1960b. A proposed standard system of nomenclature of human mitotic chromosomes (letter to the editor). American Journal of Human Genetics 12(4):384-388.
73. Down, J. Langdon. 1995. Observations on an ethnic classification of idiots. Mental Retardation 33(1):54-56.
74. Ehrlich, Paul. 1971. The population bomb. New York: Ballantine.
75. Emery, Alan E. H. 1995. The history of a genetic disease: Duchenne muscular dystrophy or Meryon's disease. London: Royal Society of Medicine Press.
76. Epstein, Steven. 1996. Impure science: AIDS, activism, and the politics of knowledge. Berkeley and Los Angeles: University of California Press.
77. Essen-Möller, E. 1970. The twin register of Lund. Acta Geneticae Medicae et Gemellologiae 19:355.
78. Faden, Ruth R., Neil Holtzman, and Judith Chwalow. 1982. Parental rights, child welfare and public health: The case of PKU screening. American Journal of Public Health 72(12):1396-1400.
79. Farber, Susan. 1981. Identical twins reared apart: A reanalysis. New York: Basic Books.
80. Ferguson-Smith, M. A. 1962. The identification of human chromosomes. Proceedings of the Royal Society of Medicine 55:471-475.
81. Ferguson-Smith, M. A., Marie E. Ferguson-Smith, Patricia M. Ellis, and Marion Dickson. 1962. The sites and relative frequencies of secondary constrictions in human somatic chromosomes. Cytogenetics 1:325-343.
82. Ferguson-Smith, M. A., A. W. Johnston, and A. N. Weinberg. 1960. Primary amentia and micro-orchidism associated with a XXXY sex chromosome constitution. Lancet 2:184-187.
83. Fisher Family. 1957. Descendants and history of Christian Fisher family. Ronks, PA: Amos L. Fisher.
84. Følling, Asbjørn. 1934. Phenylpyruvic acid as a metabolic anomaly in connection with imbecility. Nordisk Med Tidskrift 8:1054-1059.
85. Ford, C. E., and J. L. Hamerton. 1956. A colchicine, hypotonic citrate squash sequence for mammalian chromosomes. Stain Technology 31:247-251.
86. Ford, C. E., P. A. Jacobs, and L. G. Lajtha. 1958. Human somatic chromosomes. Nature 181:1565.
87. Ford, C. E., K. W. Jones, O. J. Miller, U. Mittwoch, L. S. Penrose, M. Ridler, and A. Shapiro. 1959. The chromosomes in a patient showing both mongolism and Klinefelter syndrome. Lancet 1:709-710.
88. Forster, W., and M. Tyndel. 1956. The neuropsychiatric aspects of familial dysautonomia (Riley-Day syndrome). Journal of Mental Science 102:345.
89. Franklin, Sarah. 2003. Rethinking nature-culture: anthropology and the new genetics. Anthropological Theory 3(1):65-85.
90. Franklin, Sarah, and Margaret Lock, eds. 2003. Remaking life and death: Toward an anthropology of the biosciences. Santa Fe: School of American Research Press.
91. Fraumeni, Joseph. 2000. The gene versus environment debate. Linkage (newsletter of the Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda) 11(Dec):1-2.
92. Freeman, A. M., W. Heine, and J. Havel. 1957. Psychological aspects of familial dysautonomia. American Journal of Orthopsychiatry 27:96.
93. Freireich, Emil, and Hagop Kantarjian, eds. 1993. Leukemia: Advances in research and treatment. Boston: Kluwer Academic.
94. Fujimura, Joan H. 1996. Crafting science: A sociohistory of the quest for the genetics of cancer. Cambridge: Harvard University Press.
95. Fuller, John L., and W. Robert Thompson. 1960. Behavior genetics. New York: Wiley.
96. Galton, Francis. 1874. English men of science: Their nature and nurture. London: Macmillan. Facsimile edition, Bristol, England: Thoemmes, 1998.
97. -. 1875. The history of twins as a criterion of the relative powers of nature and nurture. Fraser's Magazine 12:566-576.
98. Garrod, Archibald E. 1909. Inborn errors of metabolism. Oxford: Academic Press.
99. Garwood, D. S., and B. Augenbraun. 1968. Coordinated psychotherapeutic approaches to a familial dysautonomic preschool boy and his parents. Psychoanalytic Review 55:62.
100. Gedda, Luigi, Paolo Parisi, and Walter E. Nance, eds. 1981. Twin research 3: Proceedings of the Third International Congress on Twin Studies (3 vols). New York: Alan R. Liss.
101. Gerhard, D. S., M. C. La Buda, S. D. Bland, C. Allen, J. A. Egeland, and D. L. Pauls. 1994. Initial report of a genome search for the affective disorder predisposition gene in the old order Amish pedigrees: Chromosomes 1 and 11. American Journal of Medical Genetics 54(4):398-404.
102. Giannelli, F., and R. M. Howlett. 1966. The identification of the chromosomes of the D group (13-15) Denver: An autoradiographic and measurement study. Cytogenetics 5:186-205.
103. Gilbert, C. S. 1966. A computer program for the analysis of human chromosomes. Nature 212:1437-1440.
104. Gilbert, Scott. 1997. Bodies of knowledge: Biology and the intercultural university. In Changing life: Genomes, ecologies, bodies, commodities, ed. Peter J. Taylor, Saul E. Halfon, and Paul N. Edwards, 36-55. Minneapolis: University of Minnesota Press.
105. Ginns, E. I., J. Ott, J. A. Egeland, C. R. Allen, C. S. Fann, D. L. Pauls, J. Weissenbachoff J. P. Carulli, K. M. Falls, T. P. Keith, and S. M. Paul. 1996. A genomewide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish. Nature Genetics 12(4):431-435.
106. Ginsburg, Faye, and Rayna Rapp. 1999. Fetal reflections: Confessions of two feminist anthropologists as mutual informants. In Fetal positions/Feminist practices, ed. Lynn Morgan and Meredith Michaels, 279-295. Philadelphia: University of Pennsylvania Press.
107. Glass, Bentley. 1988. A guide to the genetics collections of the American Philosophical Society. Philadelphia: American Philosophical Society Library.
108. Goedde, H. W, and D. P. Agarwal, eds. 1987. Genetics and alcoholism. New York: Alan R. Liss.
109. -. 1989. Alcoholism: Biomedical and genetic aspects. New York: Pergamon Press.
110. Goldsmith, H. Hill. 1991. A zygosity questionnaire for young twins: A research note. Behavior Genetics 21(3):257-269.
111. Goodman, Richard M. 1979. Genetic disorders among the Jewish people. Baltimore: Johns Hopkins University Press.
112. Goodwin, D. W. 1979. Alcoholism and heredity: A review and hypothesis. Archives of General Psychiatry 36:57-61.
113. Gottesman, Irving I. 1984. Eliot Slater (1904-1983): An appreciation. Behavior Genetics 14(2):107-110.
114. Gottesman, I., and A. Bertelsen. 1996. The legacy of German psychiatric genetics: Hindsight is always 20/20. American Journal of Medical Genetics (Neuropsychiatric Genetics) 67:317-322.
115. Gottesman, Irving I., and J. Shields. 1972. Schizophrenia and genetics: A twin study vantage point. New York: Academic Press.
116. Gottesman, Michael. 2003. Cancer gene therapy: An awkward adolescence. Cancer Gene Therapy 10(7):501-508.
117. Gottweiss, Herbert. 1998. Governing molecules: The discursive politics of genetic engineering in Europe and the United States. Cambridge, MA: MIT Press.
118. Guthrie, Robert. 1961. Blood screening for phenylketonuria (letter to the editor). Journal of the American Medical Association 178:863.
119. Guthrie, Robert, and Ada Susi. 1963. A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants. Pediatrics 32:338-343.
120. Guthrie, Robert, and H. Tieckelmann. 1962. The inhibition assay: Its use in screening urinary specimens for metabolic differences associated with mental retardation. In Proceedings of the London Conference on the Scientific Study of Mental Deficiency, 672-677. London: May and Baker.
121. Guthrie, Robert, and Stewart Whitney. 1964. Phenylketonuria: Detection in the newborn infant as a routine hospital procedure. Washington, DC: Children's Bureau, U. S. Department of Health, Education and Welfare.
122. Hamerton, John. L. 1971. Human cytogenetics. New York: Academic Press.
123. Hamlin, Christopher, and Philip T. Shepard. 1993. Deep disagreement in U. S. agriculture: Making sense of policy conflict. Boulder, CO: Westview
124. Haraway Donna. 2003. For the love of a good dog: Webs of action in the world of dog genetics. In Genetic nature/culture: Anthropology and science beyond the two culture divide, ed. Alan Goodman, Deborah Heath, and Susan Lindee, 111-131. Berkeley and Los Angeles: University of California Press.
125. Harris, Harry. 1959. Human biochemical genetics. Cambridge: Cambridge University Press.
126. -. 1975. Prenatal diagnosis and selective abortion. Cambridge: Harvard University Press.
127. Hauge M., B. Harvald, M. Fischer, K. Gotlieb-Jensen, N. Juel-Nielsen, I. Raebild, R. Shapiro, and T. Videbech T. 1968. The Danish twin register. Acta Geneticae Medicae et Gemellologiae 17(2):315-332.
128. Hayes, Richard. 2002. The market for modified humans. World Watch 15(4):11-12.
129. Heath, Andrew C, Pamela A. F. Madden, and Kathleen K. Bucholz. 1999. Ascertainment of a twin sample by computerized record matching, with assessment of possible sampling biases. Behavior Genetics 29(4):209-219.
130. Henkin, R. I., and I. J. Kopin. 1964. Abnormalities of taste and smell thresholds in familial dysautonomia: Improvement with methacholine. Life Sciences 3:1319-1325.
131. Hessenbruch, Arne. 1999. The spread of precision measurement in Scandinavia, 1660-1800. In Sciences in the European periphery during the enlightenment, ed. Kostas Gavroglu, 179-224. Dordrecht, Netherlands: Kluwer.
132. Hilgartner, Stephen. 1998. Data access policy in genome research. In Private science: Biotechnology and the rise of the molecular sciences, ed. Arnold Thackray. Philadelphia: University of Pennsylvania Press.
133. Hisada, Michie, Judy Garber, Clair Fung, Joseph Fraumeni, and Frederick Li. 1998. Multiple primary cancers in families with Li-Fraumeni syndrome. Journal of the National Cancer Institute 90(8):606-611.
134. Horner, F., and C. Streamer. 1956. Effects of phenylalanine-restricted diet on patients with phenylketonuria: Clinical observations in three cases. Journal of the American Medical Association 161:1628-1630.
135. Hostetler, J. A. 1963. Amish society. Baltimore: Johns Hopkins University Press.
136. -. 1963-1964. Folk and scientific medicine in Amish society. Human Organization 22(4):269-275.
137. Hrubec, Zdenek, and James V. Neel. 1978. The National Academy of Sciences-National Research Council Twin Registry: Ten years of operation. In Twin research: Proceedings of the Second International Congress on Twin Studies, August 29-September 1, 1977, Washington, D. C., ed. Walter E. Nance; assoc. eds Gordon Allen and Paolo Parisi, 153-172. New York: Alan R. Liss.
138. Hsia, David Yi-Yung. 1960. Recent developments in inborn errors of metabolism. Journal of Public Health 50(10):1653-1661.
139. Hsu, T. C. 1952. Mammalian chromosomes in vitro: I. The karyotype of man. Journal of Heredity 43:167-172.
140. -. 1979. Human and mammalian cytogenetics: An historical perspective. Berlin: Springer-Verlag.
141. Hungerford, David. 1961. A study of the chromosomes in leukocytes from the peripheral blood of children with leukemia (Ph. D. diss., University of Pennsylvania).
142. Hungerford, D. A., S. Makino, M. Sasaki, A. A. Awa, and Gloria Balaban. 1969. Chromosome studies of the Ainu population of Hokkaido. Cytogenetics 8:74-79.
143. Hunt, Bruce J. 1994. The Ohm is where the art is: British telegraph engineers and the development of electrical standards. Osiris 9:48-63.
144. Jablon, Seymour, James V. Neel, H. Gershowitz, and G. F. Atkinson. 1967. The NAS-NRC Twin Panel: Methods of construction of the panel, zygosity diagnosis and proposed uses. American Journal of Human Genetics 19(Mar):133-161.
145. Jacobs, Paul. 2000. A father's mission. San Jose Mercury News, 31 Dec.
146. Jacobs, P. A., A. G. Baikia, W. M. Court-Brown, D. M. MacGregor, M. MacLean, and D. G. Harnden. 1959. Evidence for the existence of a human "super female." Lancet 2:423-425.
147. Jacobs, P. A., D. G. Harnden, W. M. Court Brown, J. Goldstein, H. G. Close, T. N. Macgregor, N. Maclean, and J. A. Strong. 1960. Abnormalities involving the X-chromosome in women. Lancet 1:1213-1216.
148. Jensen, Arthur. 1969. How much can we boost IQ and scholastic achievement? Harvard Educational Review 19(Feb.):1-123.
149. -. 1974. Kinship correlations reported by Sir Cyril Burt. Behavior Genetics 4(1):1-28.
150. Jervis, George. 1966. Overall view of our biochemical knowledge of PKU. In Phenylketonuria and allied metabolic diseases, ed. John A. Anderson and Kenneth F. Swaiman, 33. Washington, DC: U. S. Children's Bureau.
151. Kaback, Michael. 1977. Tay Sachs disease: Screening and prevention. New York: John Wiley and Sons.
152. Kaij, Lennart. 1960. Alcoholism in twins. Stockholm: Almqvist and Wiksell International.
153. Kallmann, Franz J. 1938. The genetics of schizophrenia: A study of heredity and reproduction in the families of 1, 087 schizophrenics, with the assistance of Senta Jonas Rypins and introduction by Nolan D. C. Lewis. New York: J. J. Augustin.
154. -. 1946. The genetic theory of schizophrenia: An analysis of 691 schizophrenic twin index families. American Journal of Psychiatry 103:309-322.
155. -. 1950a. The genetics of psychoses: An analysis of 1, 232 twin index families. American Journal of Human Genetics 2:385-390.
156. -. 1950b. The genetics of psychoses: An analysis of 1, 232 twin index families. In Congres internationale de psychiatrie, 1-27. Paris: Herman.
157. -. 1952. Human genetics as a science, as a profession, and as a social-minded trend of orientation. American Journal of Human Genetics 4(4):237-245.
158. -. 1953. Heredity in health and mental disorder: Principles of psychiatric genetics in the light of comparative twin studies, with foreword by Nolan D. C. Lewis. New York: W W Norton.
159. Kallmann, F. J., J. Deporte, E. Deporte, and L. Feingold. 1949. Suicide in twins and only children. American Journal of Human Genetics 1:113-126.
160. Kay, Lily E. 1993. The molecular vision of life: Caltech, the Rockefeller Foundation and the rise of the new biology. New York: Oxford University Press.
161. -. 2000. Who wrote the book of life? A history of the genetic code. Stanford: Stanford University Press.
162. Keller, Evelyn Fox. 1995. Refiguring life: Metaphors of 20th-century biology. New York: Columbia University Press.
163. -. 2000. The century of the gene. London: Harvard University Press.
164. Kevles, Daniel J. 1985. In the name of eugenics: Genetics and the uses of human heredity. New York: Alfred A. Knopf.
165. Kevles, Daniel J., and Leroy Hood, eds. 1992. The code of codes: Scientific and social issues in the Human Genome Project. Cambridge: Harvard University Press.
166. Klinger, Harold P., and Orlando J. Miller. 1968. Prenatal sex chromatin and chromosome analysis. In Diagnosis and treatment of fetal disorders, ed. Karlis Adamsons, 72-82. New York: Springer-Verlag.
167. Koch, Jean Holt. 1997. Robert Guthrie: The PKU story. Pasadena, CA: Hope Publishing.
168. Kohler, Robert. 1994. Lords of the fly: Drosophila genetics and the experimental life. Chicago: University of Chicago Press.
169. Kolata, Gina. 1996. Parents take charge, putting gene hunt onto the fast track. New York Times, 16 July.
170. Kottler, Malcolm J. 1974. From 48 to 46: Cytological technique, preconception and the counting of human chromosomes. Bulletin of the History of Medicine 48:467-471.
171. Kritchman, Marilyn M., Herman Schwartz, and Emanuel M. Papper. 1959. Experiences with general anesthesia in patients with familial dysautonomia. Journal of the American Medical Association 170(5):529-533.
172. Kuklick, Henrika, and Robert Kohler. 1996. Introduction. In Science in the field, vol. 11 of Osiris, 2nd ser., ed. Henrika Kuklick and Robert Kohler, 1-14. Chicago: University of Chicago Press.
173. La Buda, M. C, M. Maldonado, D. Marshall, K. Otten, and D. S. Gerhard. 1996. A follow-up report of a genome search for affective disorder predisposition loci in the Old Order Amish. American Journal of Human Genetics 59(6):1343-1362.
174. La Du, Bert N., R. Rodney Howell, Patricia J. Michael, and Eva K. Sober. 1963. A quantitative micromethod for the determination of phenylalanine in blood and its application to the diagnosis of phenylketonuria in infants. Pediatrics 31(1):39-57.
175. Lawrence, M. M. 1956. Comprehensive approach to study of a case of familial dysautonomia. Psychoanalytic Review 43:358.
176. Lejeune, J., M. Gautier, and R. Turpin. 1959a. Les chromosomes humane en culture de tissus. Comptes Rendus de l'Academie de Sciences 248:602-603.
177. -. 1959b. The chromosomes of man. Lancet 1:885.
178. -. 1959c. Etude des chromosomes somatiques de neuf enfants mongoliens. Comptes Rendus de l'Academie de Sciences 248:1721-1722.
179. Lejeune, Jerome, and Raymond Turpin. 1961. Chromosomal aberrations in man (originally presented as part of a symposium on genetics held at Western Reserve University, 10-12 Oct., 1960). American Journal of Human Genetics 13(Mar.):175-183.
180. Lejeune, Jerome, Raymond Turpin, and Marthe Gautier. 1959. Mongolisme: une maladie chromosomique (trisomy). Bulletin de l'Academie Nationale de Medecine 143:256-265.
181. Lennox, Bernard 1961. Chromosomes for beginners. Lancet, 31 May, 1046-1051.
182. Le Saux, O., K. Beck, C. Sachsinger, C. Silvestri, C. Treiber, H. H. Goring, E. W. Johnson, A. De Paepe, F. M. Pope, I. Pasquali-Ronchetti, L. Bercovitch, A. S. Marais, D. L. Viljoen, S. F. Terry, and C. D. Boyd. 2001. A spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticum. American Journal of Human Genetics 69(4):749-764.
183. Levan, Albert, and T. C. Hsu. 1959. The human idiogram. Hereditas 45:665-674.
184. Lewis, Margaret Reed. 1932. Reversible solution of the mitotic spindle of living chick embryo cells studied in vitro. Archives für Experimentelle Zellforschung 16:159-166.
185. Li, Frederick, and Joseph Fraumeni. 1969. Soft-tissue sarcomas, breast cancer, and other neoplasms: A familial syndrome? Annals of Internal Medicine 71(4):747-752.
186. Li, J. G., and E. E. Osgood. 1949. A method for the rapid separation of leukocytes and nucleated erthrocytes from blood or marrow with a phytohemagglutinin from red beans (Phaseolus vulgaris). Blood 4:670-675.
187. Lichtenstein, P., H. V. Holm, P. K. Verkasalo, et al. 2000. Environmental and heritable factors in the causation of cancer-analyses of cohorts of twins from Sweden, Denmark, and Finland. New England Journal of Medicine 343:78-85.
188. Liebler, Daniel C. 2002. Proteomics: An introduction to the new biology. Totowa, NJ: Humana.
189. Liebman, Sumner D. 1957. Riley-Day syndrome (familial dysautonomia): Concerning the etiology of the corneal pathology; an ocular survey of nineteen cases. Archives of Ophthalmology 58(6):188-192.
190. Lindee, M. Susan. 1994. Suffering made real: American science and the survivors at Hiroshima. Chicago: University of Chicago Press.
191. -. 2002. Genetic disease in the 1960s: A structural revolution. American Journal of Medical Genetics 115(2):75-82.
192. -. 2003. Voices of the dead: James Neel's Amerindian studies. In Lost paradises and the ethics of research and publication, ed. Francisco Salzano and Magdalene Hurtado, 40-73. New York: Oxford University Press.
193. Loehlin, John C, and R. C. Nichols. 1976. Heredity, environment and personality. Austin: University of Texas Press.
194. London Conference on the Normal Human Karyotype. 1963. Cytogenetics 2:264-268.
195. Luxenburger, H. 1930. Psychiatrische-Neurologische Zwillingspathologie. Zentralblatt für die Gesamte: Neurologische Psychiatrie 56:145.
196. Mabry, C. C, J. C. Denniston, T. L. Nelson, and C. D. Son. 1963. Maternal phenylketonuria: A cause of mental retardation in children without the metabolic disorder. New England Journal of Medicine 275:1331-1336.
197. Mackta, Jayne. 1992. Integrating consumers into the regional genetics networks. Chevy Chase, MD: Alliance of Genetic Support Groups.
198. Marks, Jonathan. 2002. What it means to be 98 percent chimpanzee: Apes, people, and their genes. Berkeley: University of California Press.
199. Marshall, E. Jane, and Robin M. Murray. 1989. The contribution of twin studies to alcoholism research. In Alcoholism: Biomedical and genetic aspects, ed. H. W. Goedde and D. P. Agarwal, 277-289. New York: Pergamon Press.
200. Martin, Aryn. 2004. Can't anybody count? Counting as an epistemic theme in the history of human chromosomes. Social Studies of Science 34(4):1-26.
201. Mazumdar, Pauline H. 1996. Two models for human genetics: Blood grouping and psychiatry in Germany between the World Wars. Bulletin of the History of Medicine 70:609-657.
202. McKusick, Victor A. 1949. Broedel's ulnar palsy, with unpublished Broedel sketches. Bulletin of the History of Medicine 23:469-479.
203. -. 1954. The cardiovascular and genetic aspects of Marfan's syndrome, a heritable disorder of connective tissue. Bulletin of the Johns Hopkins Hospital 94:159-161.
204. -. 1956. Heritable disorders of connective tissue. St. Louis: Mosby.
205. -. 1958. Cardiovascular sound in health and disease. Baltimore: Williams and Wilkins.
206. -. 1962 On the X chromosome of man. Quarterly Review of Biology 37:69-175.
207. -. 1964. On the X chromosome of man. Washington, DC: American Institute of Biological Science.
208. -. 1966 and various years. Mendelian inheritance in man. Baltimore: Johns Hopkins University Press. www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=omim.
209. -. 1969. On lumpers and splitters, or the nosology of genetic disease. Perspectives in Biology and Medicine 12(2):298-312.
210. -. 1973. Medical genetics. New York: H. P. Publishing.
211. -. s1978. Medical genetic studies of the Amish: Selected papers assembled with commentary. Baltimore: Johns Hopkins University Press.
212. -. 1981 The last twenty years: An overview of advances in medical genetics. In Mammalian genetics and cancer: The Jackson Laboratory Fiftieth
213. -. 1992. Human genetics: The last 35 years, the present and the future. American Journal of Human Genetics 50:663-670.
214. -. 1993. Heritable disorders of connective tissue, 5th ed. St. Louis: Mosby.
215. -. 1996. History of medical genetics. In Principles and practices of human genetics, ed. D. L. Rimoin, J. M. Connor, and R. E. Pyeritz, xiii-xviii. Edinburgh: Churchill Livingston.
216. -. 2000. Ellis-van Creveld syndrome and the Amish. Nature Genetics 24:203-204.
217. McKusick, V. A., R. Eldridge, J. A. Hostetler, U. Ruangwit, and J. A. Egeland. 1964a. Dwarfism in the Amish: I. The Ellis van Creveld syndrome. Bulletin of the Johns Hopkins Hospital 115:306-336.
218. -. 1964b Dwarfism in the Amish: II. Cartilage-hair hypoplasia. Bulletin of the Johns Hopkins Hospital 116:285-326.
219. McKusick, V. A., J. A. Hostetler, and Janice A. Egeland 1964. Genetic studies of the Amish: Background and potentialities. Bulletin of the Johns Hopkins Hospital 115:203-222.
220. McKusick, V. A., J. A. Hostetler, J. A. Egeland, and R. Eldridge. 1964. The distribution of certain genes in the Old Order Amish. Cold Spring Harbor Symposia on Quantitative Biology 29:99-113.
221. Medin, Douglas L., and Scott Atran. 1999. Folkbiology. Cambridge, MA: MIT Press.
222. Mendelsohn, Everett, Judith Swazey, and Irene Taviss, eds. 1971. Human aspects of biomedical innovation. Cambridge: Harvard University Press.
223. Menees, T. O., J. D. Miller, and L. E. Holly. 1930. Amniography: Preliminary report. American Journal of Roentgenology and Radiation Therapy 24:363-366.
224. Merriman, Curtis. 1924. The intellectual resemblance of twins. Princeton: Psychological Review Co.
225. Miller, Fiona. 1999. A blueprint for defining health: Making medical genetics in Canada, 1930s-1970s (Ph. D. Diss., York University, Toronto).
226. Milunsky Aubrey. 1973. The prenatal diagnosis of hereditary disorders. Springfield, IL: Charles C Thomas.
227. -. ed. 1979 and various years. Genetic disorders and the fetus: Diagnosis, prevention and treatment. New York: Plenum Press. Second ed., 1986; 3rd, 4th, 5th eds, Baltimore: Johns Hopkins University Press, 1992, 1998, 2004.
228. Moloshek, R. E., and J. E. Moseley 1956. Familial dysautonomia: Pulmonary manifestations. Pediatrics 17:327.
229. Moorhead, P. S., P. C. Nowell, W. J. Mellman, D. M. Battips, and D. A. Hungerford. 1960. Chromosome preparation of leukocytes cultured from human peripheral blood. Experimental Cell Research 20:613-616.
230. Morange, Michel. 1998. A history of molecular biology, trans. Matthew Cobb and Michel Morange. Cambridge: Harvard University Press.
231. Moses, S. W., Y. Rotem, N. Jagoda, N. Talmor, F. Eichhorn, and S. Levin. 1967. A clinical, genetic and biochemical study of familial dysautonomia in Israel. Israel Journal of Medical Science 3:358.
232. Motulsky, Arno. 1971. The William Allen Memorial Award Lecture: Human and medical genetics: A scientific discipline and an expanding horizon. American Journal of Human Genetics 23(2):107-123.
233. Mourant, A. E., Ada C. Kopec, and Kazimiera Domaniewska-Sobczak. 1978. The genetics of the Jews. New York: Clarendon Press.
234. Muench, Karl H. 1988. Genetic medicine. New York: Elsevier.
235. Muldal, S., and Ch. H. Ockey. 1961. The Denver classification and group II. Lancet 2:462-463.
236. Muller, H. J. 1925. Mental traits and heredity. Journal of Heredity 16:433-448.
237. -. 1949. Progress and prospects in human genetics. American Journal of Human Genetics 1(Sept.):1-18.
238. Muller-Hill, Benno. 1998. Murderous science: Elimination by scientific selection of Jews, gypsies and others in Germany, 1933-1945. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press.
239. Nance, Walter E., ed. 1978. Twin research: Proceedings of the Second International Congress on Twin Studies, August 29-September 1, 1977, Washington, D. C., assoc. eds Gordon Allen and Paolo Parisi. New York: Alan R. Liss.
240. Nathan, David G. 1995. Genes, blood and courage: A boy called Immortal Sword. Cambridge: Belknap Press of Harvard University Press.
241. National Foundation for Jewish Genetic Diseases. 1980. You have a right to know⋯ about Jewish genetic disease. New York: The Foundation.
242. National Panel of Consultants on the Conquest of Cancer. 1971. National Program for the Conquest of Cancer: Report to the Committee on Labor and Public Welfare, U. S. Senate. Washington, DC: Government Printing Office.
243. National Tay-Sachs and Allied Diseases Association. 1994. The home care book: A parents guide to caring for children with progressive neurological diseases. Brookline, MA: The Association.
244. Neel, James V. 1949. The inheritance of sickle cell anemia. Science 110:64-66.
245. -. 1994. Physician to the gene pool. New York: Wiley.
246. Neel, J. V., M. Shaw, and W. J. Schull. 1965. Genetics and epidemiology of chronic diseases (Public Health Service Bulletin No. 1163). Washington, DC: US Public Health Service.
247. Nelkin, Dorothy, and M. Susan Lindee. 1995. The DNA mystique: The gene as a cultural icon. New York: W H. Freeman.
248. Neurath, P. W, ed. 1967. I-CAN International-Chromosome Analysis Newsletter, no. 105. Vienna: International Atomic Energy Agency.
249. Neurath, P. W., and K. Enslein. 1969. Human chromosome analysis as computed from arm lengths measurement. Cytogenetics 8:337-354.
250. Newman, Horatio, Frank Freeman, and Karl Holzinger. 1937. Twins. Chicago: University of Chicago Press.
251. New York State Department of Health. 1980. The Dysautonomia Treatment and Evaluation Center at NYU Medical Center. Genesis (newsletter of the Genetics Network of the Empire State) 11:2.
252. Nora, James J., F. Clarke Fraser, John Bear, Cheryl R. Greenberg, David Patterson, and Dorothy Warburton. 1994. Medical genetics: Principles and practices, 4th ed. Philadelphia: Lea and Febiger.
253. Nowell, Peter. 1998. Cancer genetics, cytogenetics: Defining the enemy within (personal essay). Nature Medicine 4(10):1107-1108.
254. Nukaga, Yoshio, and Alberto Cambrosio. 1997. Medical pedigrees and the visual production of family disease in Canadian and Japanese genetic counseling practice. In The sociology of medical science and technology, ed. Mary Ann Elston, 29-55. Oxford: Blackwell.
255. Page, W. F. 1995. Annotation: The National Academy of Sciences-National Research Council Twin Registry. American Journal of Public Health 85:617-618.
256. Painter, T S. 1921. The Y chromosome in mammals. Science 53:503-504.
257. -. 1923. Studies in mammalian spermatogenesis: II. The spermatogenesis of man. Journal of Experimental Zoology 37:291-334.
258. Paris Conference. 1971. Standardization in human cytogenetics. Birth Defects Original Article Series 8:7.
259. Reprinted in Cytogenetics 11(1972):313-362.
260. Parisi, P., and M. Di Bacco. 1968. Fingerprints and the diagnosis of zygosity in twins. Acta Geneticae Medicae et Gemellologiae 17(2):333-358.
261. Partanen, J., K. Bruun, and T. Markkanen. 1966. Inheritance of drinking behavior. Helsinki: Finnish Foundation for Alcohol Studies.
262. Patau, Klaus. 1960. The identification of individual chromosomes, especially in man. American Journal of Human Genetics 12:250-276.
263. -. 1961. Chromosome identification and the Denver report. Lancet 1:933-934.
264. -. 1963. Review of John L. Hamerton, ed. Chromosomes in Man. Cytogenetics 2:269-270.
265. -. 1965. The chromosomes. Birth Defects Original Article Series 1(2):71-74.
266. Paul, Diane. 1991. The Rockefeller Foundation and the origins of behavior genetics. In The expansion of American biology, ed. Keith R. Benson, Jane Maienschein, and Ronald Rainger, 262-283. New Brunswick, NJ: Rutgers University Press.
267. -. 1995. Controlling human heredity, 1865 to the present. Atlantic Highlands, NJ: Humanities Press.
268. -. 1998. The politics of human heredity: Essays on eugenics, biomedicine and the nature-nurture debate. Albany: State University of New York Press.
269. -. 1999a. Contesting consent: the challenge to compulsory neonatal screening for PKU. Perspectives in Biology and Medicine 24(2):207-219.
270. -. 1999b. Report on the history of newborn screening. In Promoting safe and effective genetic testing in the United States: Final report, Task Force on Genetic Testing, ed. Neil A. Holtzman and Michael S. Watson. Baltimore: Johns Hopkins University Press. (Orig. pub. Washington DC: National Institutes of Health-Department of Energy Working Group on Ethical, Legal and Social Implications of Human Genome Research, 1997.)
271. Paul, Diane, and Paul J. Edelson. 1998. The struggle over metabolic screening. In Molecularizing biology and medicine: New practices and alliances, 1910s-1970s, ed. Soraya de Chadarevian and Harmke Kamminga, 203-220. Amsterdam: Harwood Academic.
272. Pearson, J., L. Brandeis, and A. C. Cuello. 1982. Depletion of substance P-containing axons in substantia gelatinosa of patients with diminished pain sensitivity. Nature 295:61-63.
273. Pearson, J., G. Budzilovich, and M. J. Finegold. 1971. Sensory, motor, and autonomic dysfunction: The nervous system in familial dysautonomia. Neurology 21:486-493.
274. Peele, Stanton. 1986. The implications and limitations of genetic models of alcoholism and other addictions. Journal of Studies on Alcohol 47:63-73.
275. Peeters, Hilde, Sophie Van Gestel, Robert Vlietinck, Catherine Derom, and R. Derom. 1998. Validation of a telephone zygosity questionnaire in twins of known zygosity. Behavior Genetics 28(3):159-163.
276. Pemberton, Stephen. 2001. Normality within limits: Hemophilia, the citizen-patient and the risks of medical management in the United States of America from World War II to the age of AIDS (Ph. D. diss., University of North Carolina, Chapel Hill).
277. Penrose, Lionel. 1934. The influence of heredity on disease. London: H. K. Lewis.
278. -. 1946. Phenylketonuria: A problem in eugenics. Lancet, June 29.
279. -. 1964. A note on the mean measurements of human chromosomes. Annals of Human Genetics 28:195-196.
280. Perlman, Max, Sam Benady and Ephraim Saggi. 1979. Neonatal diagnosis of familial dysautonomia. Pediatrics 63(2):238-241.
281. Plomin, R., M. J. Owen, and P. McGuffin. 1994. The genetic basis of complex human behaviors. Science 264(5166):1733-1739.
282. Pollen, Daniel E. 1993. Hannah's heirs: The quest for the genetic origins of Alzheimer's disease. New York: Oxford University Press.
283. Porter, Ian H. 1974. Introduction. In Clinical cytogenetics and genetics: Boston conference on the diagnosis, genetics and management of birth defects, ed. Daniel Bergsma, x. New York: Stratton Intercontinental Medical Book.
284. Porter, Theodore. 1996. Trust in numbers: The pursuit of objectivity in science and public life. Princeton: Princeton University Press.
285. President's Cancer Panel. 1990. President's Cancer Panel: National Cancer Program Human gene therapy meeting. Silver Spring, MD: Eberlin Reporting Service.
286. Proctor, Robert. 1989. Racial hygiene: Medicine under the Nazis. Cambridge: Harvard University Press.
287. -. 1995. Cancer wars: How politics shapes what we know and don't know about cancer. New York: Basic Books.
288. Pyeritz, Reed. 1998. Medical genetics: End of the beginning or beginning of the end? Genetics in Medicine 1(1):56-60.
289. Rabinow, Paul. 1996. Making PCR: A history of biotechnology. Chicago: University of Chicago Press.
290. -. 1999. French DNA: Trouble in purgatory. Chicago: University of Chicago Press.
291. Rader, Karen. 2004. Making mice: Standardizing animals for American biomedical research, 1900-1955. Princeton: Princeton University Press.
292. Rapp, Rayna. 2000. Testing women, testing the fetus: The social impact of amniocentesis in America. New York: Routledge.
293. -. 2003. Cell life and death, child life and death: Genomic horizons, genetic diseases, family stories. In Remaking life and death: Toward an anthropology of the biosciences, ed. Sarah Franklin and Margaret Lock, 129-164. Santa Fe: School of American Research Press.
294. Rende, R. D., R. Plomin, and S. G. Vandenberg. 1990. Who discovered the twin method? Behavior Genetics 2(Mar. 20):277-285.
295. Riis, P., and F. Fuchs. 1960. Antenatal determination of fetal sex in prevention of hereditary diseases. Lancet 2:180-182.
296. Riley, Conrad. 1956. Living with a child with familial dysautonomia. New York: Dysautonomia Foundation.
297. -. 1964. Maturation of a clinical entity. New England Journal of Medicine 9(27 Aug.):271. (Unattributed but written by Riley, personal communication.)
298. -. 1970. A short history of familial dysautonomia (unpublished report to the Dysautonomia Association, 19 Nov.).
299. Riley, C. M., R. L. Day, D. M. Greeley, and W. S. Langford. 1949. Central autonomic dysfunction with defective lacrimation: Report of five cases. Pediatrics 3:468.
300. Riley, C. M., A. M. Freedman, and W. S. Langford. 1954. Further observations on familial dysautonomia. Pediatrics 14:475.
301. Riley, C. M., and R. H. Moore. 1966. Familial dysautonomia differentiated from related disorder: Case reports and discussions of current concepts. Pediatrics 37:43.
302. Ritvo, Harriet. 1987. The animal estate: The English and other creatures in the Victorian age. Cambridge: Harvard University Press.
303. Rosanoff A. J., L. M. Handy, and I. A. Rosanoff 1934. Etiology of epilepsy with special reference to its occurrence in twins. Archives of Neurology and Psychiatry 31:1165-1193.
304. Rosenberg, Charles E. 1997. The bitter fruit: Heredity, disease and social thought. In No other gods: On science and American social thought. Baltimore: Johns Hopkins University Press. (Orig. pub. 1976.)
305. Rothman, Barbara Katz. 1986. The tentative pregnancy: Prenatal diagnosis and the future of motherhood. New York: Viking.
306. Rowe-Richmond, La Velda, and La Vona Rowe-Richmond. 1976. The history of the International Twins Association. Acta Geneticae Medicae et Gemellologiae 25:387-388.
307. Rowley, Janet. 1973. A new consistent chromosome abnormality in chronic myelogenous leukemia. Nature 243:290-293.
308. -. 1998. Cancer genetics, cytogenetics: Defining the enemy within (personal essay). Nature Medicine 4(10):1107-1108.
309. Rubin, Berish. 2003. Tocotrienols induce IKBKAP expression: A possible therapy for familial dysautonomia. Biochemical and Biophysical Research Communications 306(1):303-309.
310. Sak, H. G., A. A. Smith, and J. Dancis. 1967. Psychometric evaluations of children with familial dysautonomia. American Journal of Psychiatry 124:5.
311. Salzano, Francisco. 1957. The blood groups of South American Indians. American Journal of Physical Anthropology 15:555-579.
312. Sandberg, Avery A. 1979. Before 1956: Some historical background to the study of chromosomes in human cancer and leukemia. Cancer Genetics and Cytogenetics 1:87-94.
313. Scarr, Sandra. 1987. Three cheers for behavior genetics: Winning the war and losing our identity. Behavior Genetics 17(3):219-228.
314. Schaffer, Simon. 1994. Rayleigh and the establishment of electrical standards. European Journal of Physics 15:277-285.
315. -. 1995. Accurate measurement is an English science. In The values of precision, ed. Norton Wise, 135-172. Princeton: Princeton University Press.
316. Schull, William J. 1990. Song among the ruins. Cambridge: Harvard University Press.
317. Scriver, Charles R. 1995. What ever happened to PKU? Clinical Biochemistry 28(2):137-144.
318. Secord, James. 1981. Nature's fancy: Charles Darwin and the breeding of pigeons. Isis 72:162-186.
319. Seixas, F. A., G. S. Omenn, E. D. Burk, and S. Eggleston, eds. 1972. Nature and Nurture in Alcoholism, vol. 197 of Annals of the New York Academy of Sciences. New York: New York Academy of Sciences.
320. Sexton, Sarah. 2002. A deceptive promise of cures for disease. World Watch 15(4):18-21.
321. Shapiro, Burton L., and Ralph C. Heusner. 1991. A parent's guide to cystic fibrosis. Minneapolis: University of Minnesota Press.
322. Shettles, L. B. 1956. Nuclear morphology of cells in human amniotic fluid in relation to the sex of the infant. American Journal of Obstetrics and Gynecology 71:834-838.
323. Siemens, Hermann W. 1924. Die Zwillingspathologie. Berlin: Springer.
324. Slater, Eliot. 1953. Psychotic and neurotic illnesses in twins, with the assistance of James Shields (Medical Research Council Special Report Series no. 278). London: Stationery Office.
325. Slaugenhaupt, Susan A., Anat Blumenfeld, Sandra P. Gill, Maire Leyne, James Mull, Math P. Cuajungco, Christopher B. Liebert, Brian Chadwick, Maria Idelson, Luba Reznik, Christiane M. Robbins, Izabele Makalowska, Michael Brownstein, Daniel Krappmann, Claus Scheidereit, Channa Maayan, Felicia B. Axelrod, and James F. Gusella. 2001. Tissue-specific expression of a splicing mutation in the IKBKAP gene causes familial dysautonomia. American Journal of Human Genetics 68:598-605.
326. Slifer, Eleanor. 1934. Insect development: VI. The behavior of grasshopper embryos in anisotonic balanced salt solutions. Journal of Experimental Zoology 67:137-157.
327. Smith, Alfred A., and Joseph Dancis. 1962. Response to intradermal histamine in familial dysautonomia: A diagnostic test. Pediatrics 63(5):889-894.
328. -. 1964a. Peripheral sensory deficits in familial dysautonomia. Journal of Pediatrics 65:1035.
329. -. 1964b. Familial pheochromocytoma presenting as familial dysautonomia. Pediatrics 65(3):463-465.
330. -. 1970. Familial dysautonomia: What's in a name? Pediatrics 77(1):174-175.
331. Smocovitis, Vassiliki. 1996. Unifying biology: The evolutionary synthesis and evolutionary biology. Princeton: Princeton University Press.
332. Snow, Herbert. 1885. Is cancer hereditary? British Medical Journal, 10 Oct., 690-692.
333. Spuhler, J. N., ed. 1967. Genetic diversity and human behavior (Viking Fund Publications in Anthropology no. 45). New York: Wenner-Gren Foundation for Anthropological Research.
334. Stern, Curt. 1949. Principles of human genetics. San Francisco: W. H. Freeman.
335. Stranahan, Susan Q. 1997. Clinic a lifeline to children: A doctor finds his calling among the Amish and Mennonites. Philadelphia Inquirer, 15 Sept.
336. Sumner, A. T 1982 The nature and mechanisms of chromosome banding. Cancer Genetics and Cytogenetics 6:59-87.
337. Task Force on Genetic Testing. 1999. Promoting safe and effective genetic testing in the United States: Final report, ed. Neil A. Holtzman and Michael S. Watson. Baltimore: Johns Hopkins University Press. (Orig. pub. Washington DC: National Institutes of Health-Department of Energy Working Group on Ethical, Legal and Social Implications of Human Genome Research, 1997.)
338. Tate, Carolyn, and Gordon Bendersky 1999. Olmec sculptures of the human fetus. Perspectives in Biology and Medicine 42(3):303-332.
339. Tauber, Miriam. 2001. Race to discover gene mutation ends in virtual tie. Forward, 17 Aug.
340. Taubman, Paul. 1976a. The determinants of earnings: Genetics, family and other environments. American Economic Review 66:858-870.
341. -. 1976b. Earnings, education, genetics and environment. Journal of Human Resources 11:447-461.
342. -. 1978. Determinants of socioeconomic success: Regression and latent variables analysis in samples of twins. In Twin research: Proceedings of the Second International Congress on Twin Studies, August 29-September 1, 1977, Washington, D. C., ed. Walter E. Nance; assoc. eds Gordon Allen and Paolo Parisi, 175-187. New York: Alan R. Liss.
343. Taussig, Karen-Sue. 2005. Molecules, medicine and bodies: Building social relationships for a molecular revolution in medicine. In Complexities: Beyond nature and nurture, ed. Susan McKinnon and Sydel Silverman. Chicago: University of Chicago Press.
344. Taussig, Karen-Sue, Rayna Rapp, and Deborah Heath. 2002. Flexible eugenics: Technologies of the self in the age of genetics. In Anthropology in the age of genetics: Practice, discourse, critique, ed. A. Goodman, D. Heath, S. Lindee, 58-76. Berkeley and Los Angeles: University of California Press.
345. Taylor, Charlotte. 1970. Marriages of twins to twins. Acta Geneticae Medicae et Gemellologiae 20:96-113.
346. Terrenato, L., M. F. Gravina, A. San Martini, and L. Ulizzi. 1981. Natural selection associated with birth weight: III. Changes over the last twenty years. Annals of Human Genetics 45:267.
347. Thompson, Larry. 2000. Human gene therapy: Harsh lessons, high hopes. FDA Consumer Magazine, Sept.-Oct.
348. Thorndike, Edward L. 1905. Measurement of twins. Archives of Philosophy, Psychology, and Scientific Methods, no. 1(Sept.):1-64.
349. Tjio, J. H., and A. Levan. 1956a. The chromosome number of man. American Journal of Obstetrics and Gynecology 130:723-724.
350. -. 1956b. The chromosome number of man. Hereditas 42:1-6.
351. Tjio, J. H., and T. T. Puck. 1958. The somatic chromosomes of man. Proceedings of the National Academy of Sciences 44:1229-1237.
352. Tjio, J. H., T. T. Puck, and A. Robinson. 1959. The somatic chromosomal constitution of some human subjects with genetic defects. Proceedings of the National Academy of Sciences 45:1008-1016.
353. Todes, Daniel P. 2002. Pavlov's physiology factory: Experiment, interpretation, laboratory enterprise. Baltimore: Johns Hopkins University Press.
354. Tufte, Edward R. 1997. Visual explanations: Images and quantities, evidence and narrative. Cheshire, CT Graphics Press.
355. Vandenberg, Steven G., ed. 1968. Progress in human behavior genetics: Recent reports on genetic syndromes, twin studies and statistical analyses. Baltimore: Johns Hopkins University Press.
356. Vandenberg, Steven G., and John C. De Fries. 1970. Our hopes for behavior genetics. Behavior Genetics 1(1):1.
357. Vogel, F., and A. G. Motulsky. 1986. Human genetics: Problems and approaches, 2nd ed. Berlin: Springer-Verlag.
358. Vullo, R., and B. Modell. 1990. What is thalassemia? New York: Cooley's Anemia Foundation.
359. Wailoo, Keith. 1997. Drawing blood: Technology and disease identity in twentieth century America. Baltimore: Johns Hopkins University Press.
360. -. 2001. Dying in the city of the blues: Sickle cell anemia and the politics of race and health. Chapel Hill: University of North Carolina Press.
361. Warburton, Dorothy, D. A. Miller, O. J. Miller, P. W. Allderdice, and A. De Capoa. 1969. Detection of minute deletions in human karyotypes. Cytogenetics 8:97-108.
362. Watson, James. 1965. The molecular biology of the gene. New York: W. A. Benjamin.
363. Weatherall, D. J. 1991. The new genetics and clinical practice. Oxford: Oxford University Press.
364. Weindling, Paul. 1989. Health, race and German politics between National Unification and Nazism, 1870-1945. Cambridge: Cambridge University Press.
365. Weiner, Charles. 1994. Anticipating the consequences of genetic engineering: Past, present and future. In Are genes us? The consequences of the new genetics, ed. Carl F. Cranor, 31-51. New Brunswick, NJ: Rutgers University Press.
366. Weiss, Joan O., and Jayne S. Mackta. 1996. Starting and sustaining genetic support groups. Baltimore: Johns Hopkins University Press.
367. Weiss, Sheila Faith. 1987. Race hygiene and national efficiency: The eugenics of Wilhelm Schallmayer. Berkeley and Los Angeles: University of California Press.
368. Welton, Wooster, David Clayson, Felicia Axelrod, and David B. Levine. 1979. Intellectual development and familial dysautonomia. Pediatrics 63(5):708-712.
369. Wexler, Alice. 1995. Mapping fate: A memoir of family, risk and genetic research. Berkeley and Los Angeles: University of California Press.
370. Wise, Norton. 1995. The values of precision. Princeton: Princeton University Press.
371. Wolfe, S. M., and R. I. Henkin. 1970. Absence of taste in type II familial dysautonomia: unresponsiveness to methacholine despite the presence of taste buds. Pediatrics 77(1):103-108.
372. Woolf Charles M., and Frank Dukepoo. 1959. Hopi Indians: Interbreeding and albinism. Science 164:30-37.
373. Woolf, L. I. 1966. Large-scale screening for metabolic disease in the newborn in Great Britain. In Phenylketonuria and allied metabolic diseases, ed. John A. Anderson and Kenneth F. Swaiman, 50-61. Washington, DC: U. S. Children's Bureau.
374. Woolf, Louis, and D. B. Vulliamy. 1951. Phenylketonuria with a study of the effect upon it of glutamic acid. Archives of Disease in Childhood 26:487-494.
375. World Health Organization. 1966. The use of twins in epidemiological studies (report of the WHO Meeting of Investigators on Methodology of Twin Studies). Acta Geneticae Medicae et Gemellologiae 15(2):113.
376. Wright, Susan. 1994. Molecular politics: Developing American and British regulatory policy for genetic engineering. Chicago: University of Chicago Press.
377. Yoxen, Edward. 1982. Constructing genetic diseases. In The problem of medical knowledge: Examining the social construction of medicine, ed. P. Wright and A. Treacher, 144-161. Edinburgh: Edinburgh University Press.
378. Zernig, Gerald, A. Saria, M. Kurz, and S. S. O'Malley 2000. Handbook of alcoholism. Boca Raton: CRC Press.
379. Zihni, Lilian S. 1995. Mongolism, Down's syndrome and trisomy 21: Damning diagnoses in the twentieth century. History and Philosophy of Psychology Newsletter 21(autumn):20-25.
380. Zonderman, A. B. 1986. Twins, families, and the psychology of individual differences: The legacy of Steven G. Vandenberg. Behavior Genetics 16:11-24.