共 11 条
[1]
Hampton M.L., Anderson J., Lavizzo B.S., Bergman A.B., Sickle cell ‘non-disease’, Am J Dis Child, 128, pp. 58-61, (1974)
[2]
McQueen D., Social aspects of genetic screening for Tay-Sachs disease: The pilot community screening program in Baltimore and Washington, Soc Biol, 22, pp. 125-133, (1975)
[3]
Goldstein M.S., Greenwald S., Nathan T., Massarik F., Kaback M.M., Health behavior and genetic screening for carriers of Tay-Sachs disease: A prospective study, Soc Sci Med, 11, pp. 515-520, (1977)
[4]
Scriver C.R., Bardanis M., Cartier L., Clow C.L., Lancaster G.A., Ostrowsky J.T., Beta-thalassemia disease prevention: Genetic medicine applied, Am J Hum Genet, 36, pp. 1024-1038, (1984)
[5]
Lustig L., Clarke S., Cunningham G., Schonberg R., Tompkinson G., California’s experience with low MSAFP results, Am J Med Genet, 31, pp. 211-222, (1988)
[6]
Annas G.J., Elias S., Maternal serum AFP: Educating physicians and the public, Am J Public Health, 75, pp. 1374-1375, (1985)
[7]
Clow C.L., Scriver C.R., Knowledge about and attitudes toward genetic screening among high school students: The Tay-Sachs experience, Pediatrics, 59, pp. 86-91, (1977)
[8]
Holtzman N.A., Genetic screening: For better or for worse?, Pediatrics, 59, pp. 131-133, (1977)
[9]
Tambor E.S., Chase G.A., Faden R.R., Geller G., Hofman K.J., Holtzman N.A., The effect of improved response rates on a survey of physicians’ knowledge and attitudes regarding genetics, Am J Pub Hlth
[10]
Hofman K.J., Tambor E.S., Chase G.A., Geller G., Faden R.R., Holtzman N.A., Physicians’ knowledge of genetics and genetic tests