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6. Ethical implications of the Human Genome Diversity Project. McPherson EC Nursingconnections; 1995; 8(1):36-43. PubMed ID: 7777074 [No Abstract] [Full Text] [Related]
7. Policy forum: health care delivery. Building populations genetics resources using the U.K. NHS. Fears R; Poste G Science; 1999 Apr; 284(5412):267-8. PubMed ID: 10232974 [No Abstract] [Full Text] [Related]
8. Group identity and human diversity: keeping biology straight from culture. Juengst ET Am J Hum Genet; 1998 Sep; 63(3):673-7. PubMed ID: 9718361 [No Abstract] [Full Text] [Related]
9. Participation in pedigree studies and the risk of impeded access to health insurance. Kass NE IRB; 1993; 15(5):7-10. PubMed ID: 11659704 [No Abstract] [Full Text] [Related]
10. Protecting communities in research: philosophical and pragmatic challenges. Weijer C Camb Q Healthc Ethics; 1999; 8(4):501-13. PubMed ID: 10513308 [No Abstract] [Full Text] [Related]
11. Roundtable: the politics of genetic testing. Charo RA; Cook-Deegan RM; Eisenberg RS; Geller G; Finneran K Issues Sci Technol; 1996; 13(1):48-54. PubMed ID: 11654760 [No Abstract] [Full Text] [Related]
12. Universal Declaration on the Human Genome and Human Rights: the first legal and ethical framework at the global level. Lenoir N Columbia Human Rights Law Rev; 1999; 30(1):537-87. PubMed ID: 12680391 [No Abstract] [Full Text] [Related]
13. The control of genetic research: involving the "groups between". Greely HT Houst Law Rev; 1997; 33(5):1397-430. PubMed ID: 12627555 [No Abstract] [Full Text] [Related]
14. Pedigrees-publish? or perish the thought? Byers PH; Ashkenas J Am J Hum Genet; 1998 Sep; 63(3):678-81. PubMed ID: 9718362 [No Abstract] [Full Text] [Related]
15. We're off to see the genome. Reilly PR; Page DC Nat Genet; 1998 Sep; 20(1):15-7. PubMed ID: 9731523 [TBL] [Abstract][Full Text] [Related]
16. An egg takes flight: the once and future life of the National Bioethics Advisory Commission. Capron AM Kennedy Inst Ethics J; 1997 Mar; 7(1):63-80. PubMed ID: 11654623 [No Abstract] [Full Text] [Related]
17. Is genetics research "minimal risk". Merz JF IRB; 1996; 18(6):7-8. PubMed ID: 11654745 [No Abstract] [Full Text] [Related]
18. Publication-related risks to privacy: ethical implications of pedigree studies. Powers M IRB; 1993; 15(4):7-11. PubMed ID: 11652150 [No Abstract] [Full Text] [Related]
19. Why the use of anonymous samples for research matters. Clayton EW J Law Med Ethics; 1995; 23(4):375-7. PubMed ID: 8715059 [No Abstract] [Full Text] [Related]
20. Should parents be permitted to authorize genetic testing for their children? Holland J Fam Law Q; 1997; 31(2):321-53. PubMed ID: 11660616 [No Abstract] [Full Text] [Related] [Next] [New Search]