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5. Custom kids and the moral duty to genetically engineer our children. Rosenkranz EJ High Technol Law J; 1987; 2(1):1-53. PubMed ID: 11659156 [No Abstract] [Full Text] [Related]
6. Who should pay for bad genes? Rakowski E Calif Law Rev; 2002 Oct; 90(5):1345-414. PubMed ID: 12436972 [TBL] [Abstract][Full Text] [Related]
7. Will the baby be normal? And what is the cost of knowing. Hilton B Hastings Cent Rep; 1972 Jun; 2(3):8-9. PubMed ID: 4679744 [No Abstract] [Full Text] [Related]
8. Options in dealing with the threat of hemophilia. Bok S; Lappe M Hastings Cent Rep; 1974 Apr; 4(2):8-9. PubMed ID: 4414935 [No Abstract] [Full Text] [Related]
9. Amniocentesis: a case study in the management of "genetic engineering". Etzioni A Ethics Sci Med; 1975 May; 2(1):13-24. PubMed ID: 1061671 [No Abstract] [Full Text] [Related]
10. Mother matters: a fresh look at prenatal genetic testing. Lippman A Issues Reprod Genet Eng; 1992; 5(2):141-54. PubMed ID: 11653996 [No Abstract] [Full Text] [Related]
11. Genetics and responsible parenthood. Häring B Soc Thought; 1976; 2(3):7-13. PubMed ID: 11651682 [No Abstract] [Full Text] [Related]
12. Prenatal screening: professional standards and the limits of parental choice. Botkin JR Obstet Gynecol; 1990 May; 75(5):875-80. PubMed ID: 2109295 [TBL] [Abstract][Full Text] [Related]
13. In search of the perfect child: genetic testing and selective abortion. Peters T Christ Century; 1996 Oct; 113(31):1034-7. PubMed ID: 11656621 [No Abstract] [Full Text] [Related]
14. Frontiers of genetic research: science and religion. Friend W Origins; 1995 Jan; 24(31):522-8. PubMed ID: 11659914 [No Abstract] [Full Text] [Related]
15. Making responsible decisions. An interpretive ethic for genetic decisionmaking. White MT Hastings Cent Rep; 1999; 29(1):14-21. PubMed ID: 10052006 [No Abstract] [Full Text] [Related]
16. Responding to persons: methods of moral argument in debate over abortion. Noonan JT Theol Dig; 1973; 21(4):291-307. PubMed ID: 11660973 [No Abstract] [Full Text] [Related]
17. Ethical considerations in the social context of Huntington disease. Turner D Dis Markers; 1992; 10(4):171-83; discussion 211-28. PubMed ID: 1304435 [No Abstract] [Full Text] [Related]
18. Rights discourse and neonatal euthanasia. Schneider CE Calif Law Rev; 1988 Jan; 76(1):151-76. PubMed ID: 11659061 [No Abstract] [Full Text] [Related]
19. The ethical and legal implications of genetic screening, counseling, and treatment. Spring CM Relig Humanism; 1974; 8(4):177-82. PubMed ID: 11663257 [No Abstract] [Full Text] [Related]