158 related articles for article (PubMed ID: 8669508)
1. Nonconsensual participation in genetic studies.
Lippman A
Am J Public Health; 1996 Jul; 86(7):1030. PubMed ID: 8669508
[No Abstract] [Full Text] [Related]
2. Research and stored tissues. Persons as sources, samples as persons?
Knoppers BM; Laberge CM
JAMA; 1995 Dec; 274(22):1806-7. PubMed ID: 7500515
[No Abstract] [Full Text] [Related]
3. Pathologists enter debate on consent for genetic research on stored tissue.
Stephenson J
JAMA; 1996 Feb; 275(7):503-4. PubMed ID: 8606455
[No Abstract] [Full Text] [Related]
4. Iceland OKs private health databank.
Enserink M
Science; 1999 Jan; 283(5398):13. PubMed ID: 9917253
[No Abstract] [Full Text] [Related]
5. Informed consent for genetic research on stored tissue samples.
Clayton EW; Steinberg KK; Khoury MJ; Thomson E; Andrews L; Kahn MJ; Kopelman LM; Weiss JO
JAMA; 1995 Dec; 274(22):1786-92. PubMed ID: 7500511
[TBL] [Abstract][Full Text] [Related]
6. Opponents criticize Iceland's database.
Enserink M
Science; 1998 Oct; 282(5390):859. PubMed ID: 9841428
[No Abstract] [Full Text] [Related]
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]
9. Ethical and legal issues in genetic epidemiology.
Holtzman NA; Andrews LB
Epidemiol Rev; 1997; 19(1):163-74. PubMed ID: 9360913
[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]
12. Privacy in genetics research.
Fuller BP; Kahn MJ; Barr PA; Biesecker L; Crowley E; Garber J; Mansoura MK; Murphy P; Murray J; Phillips J; Rothenberg K; Rothstein M; Stopfer J; Swergold G; Weber B; Collins FK; Hudson KL
Science; 1999 Aug; 285(5432):1359-61. PubMed ID: 10490410
[No Abstract] [Full Text] [Related]
13. Iceland's database is ethically questionable.
Andersen B; Arnason E
BMJ; 1999 Jun; 318(7197):1565. PubMed ID: 10356045
[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]
18. Genetic testing and individual rights.
Handelin B; Wachbroit R; Billings P; Scheck B; Reilly P; Milunsky A
Suffolk Univ Law Rev; 1993; 27(4):1477-97. PubMed ID: 11657046
[No Abstract] [Full Text] [Related]
19. Gene donors' rights at risk.
Nature; 1996 May; 381(6577):1. PubMed ID: 8609968
[No Abstract] [Full Text] [Related]
20. Dangerous intersections.
Korn D
Issues Sci Technol; 1996; 13(1):55-62. PubMed ID: 11654761
[No Abstract] [Full Text] [Related]
[Next] [New Search]