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7. 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]
8. ASHG report. Statement on informed consent for genetic research. The American Society of Human Genetics. Am J Hum Genet; 1996 Aug; 59(2):471-4. PubMed ID: 8755936 [No Abstract] [Full Text] [Related]
10. 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]
11. A country unveils its gene pool and debate flares. Lyall S N Y Times Web; 1999 Feb; ():F1, F4. PubMed ID: 11647698 [No Abstract] [Full Text] [Related]
14. DNA banking and informed consent -- part 2. Weir RF; Horton JR IRB; 1995; 17(5-6):1-8. PubMed ID: 11653356 [No Abstract] [Full Text] [Related]
15. Storm brews over gene bank of Estonian population. Frank L Science; 1999 Nov; 286(5443):1262-3. PubMed ID: 10610525 [No Abstract] [Full Text] [Related]
16. Icelandic health records. Andersen B Science; 1998 Dec; 282(5396):1993. PubMed ID: 9874648 [No Abstract] [Full Text] [Related]
17. Genotyping in clinical trials: towards a principle of informed request. Sass HM J Med Philos; 1998 Jun; 23(3):288-96. PubMed ID: 9736190 [TBL] [Abstract][Full Text] [Related]