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3. US privacy laws may curb access to medical data. Wadman M Nature; 1997 Apr; 386(6625):533. PubMed ID: 9121564 [No Abstract] [Full Text] [Related]
4. Ethical issues in genetic research: disclosure and informed consent. Reilly PR; Boshar MF; Holtzman SH Nat Genet; 1997 Jan; 15(1):16-20. PubMed ID: 8988163 [TBL] [Abstract][Full Text] [Related]
5. The impact of the Genetic Privacy Act on medicine. Reilly PR J Law Med Ethics; 1995; 23(4):378-81. PubMed ID: 8715060 [No Abstract] [Full Text] [Related]
8. US geneticists encouraged to play by the book. Wadman M Nature; 2000 Apr; 404(6778):530. PubMed ID: 10787343 [No Abstract] [Full Text] [Related]
9. 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]
10. Privacy bill under fire from researchers. Wadman M Nature; 1998 Mar; 392(6671):6. PubMed ID: 9510231 [No Abstract] [Full Text] [Related]
12. The Genetic Privacy Act: an analysis of privacy and research concerns. Troy ES J Law Med Ethics; 1997; 25(4):256-72, 230. PubMed ID: 11066508 [TBL] [Abstract][Full Text] [Related]
13. Institutional review boards and the new privacy rule. Maloney DM Hum Res Rep; 2001 Sep; 16(9):1-3. PubMed ID: 11833565 [No Abstract] [Full Text] [Related]