290 related articles for article (PubMed ID: 7777074)
21. Principled conduct of genetics research.
Human Genome Organization. Ethical, Legal, and Social Issues Committee
Bull Med Ethics; 1996 Sep; No. 121():10-1. PubMed ID: 11654574
[No Abstract] [Full Text] [Related]
22. Informed consent: some challenges to the universal validity of the Western model.
Levine RJ
Law Med Health Care; 1991; 19(3-4):207-13. PubMed ID: 1779688
[No Abstract] [Full Text] [Related]
23. Genetics and the dead: implications for genetics research with samples from deceased persons.
DeRenzo EG; Biesecker LG; Meltzer N
Am J Med Genet; 1997 Mar; 69(3):332-4. PubMed ID: 9096766
[No Abstract] [Full Text] [Related]
24. Gene treaty promises rewards for unique peoples.
Coghlan A
New Sci; 1996 Nov; 152(2054):8. PubMed ID: 11656591
[No Abstract] [Full Text] [Related]
25. Community participation and representation in genetic studies: testing the application of fundamental ethical principles.
Brito A
St Thomas Law Rev; 2001; 13(4):935-43. PubMed ID: 12661583
[No Abstract] [Full Text] [Related]
26. Mining the genetic riches of human populations.
Brower V
Nat Biotechnol; 1998 Apr; 16(4):337-40. PubMed ID: 9555722
[No Abstract] [Full Text] [Related]
27. Rules for research on human genetic variation--lessons from Iceland.
Annas GJ
N Engl J Med; 2000 Jun; 342(24):1830-3. PubMed ID: 10853009
[No Abstract] [Full Text] [Related]
28. Interrogating the Human Diversity Genome Project.
Lock M
Soc Sci Med; 1994 Sep; 39(5):603-6. PubMed ID: 7973860
[No Abstract] [Full Text] [Related]
29. Don't confuse me with ethics: I already know what's right.
Taylor A
J Nucl Med; 1992 Feb; 33(2):296-303. PubMed ID: 1732458
[No Abstract] [Full Text] [Related]
30. Indigenous peoples and the morality of the Human Genome Diversity Project.
Dodson M; Williamson R
J Med Ethics; 1999 Apr; 25(2):204-8. PubMed ID: 10226929
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Genes from a disappearing world.
Lewin R
New Sci; 1993 May; 138(1875):25-9. PubMed ID: 11656244
[No Abstract] [Full Text] [Related]
33. Population-based genetic studies: informed consent and confidentiality.
Smith MJ
Santa Clara Comput High Technol Law J; 2001 Dec; 18(1):57-93. PubMed ID: 12741383
[No Abstract] [Full Text] [Related]
34. Issues in preparing ethical guidelines for epidemiological studies.
Dickens BM
Law Med Health Care; 1991; 19(3-4):175-83. PubMed ID: 1779685
[No Abstract] [Full Text] [Related]
35. Ethics and genetics in China: an inside story.
Mao X
Nat Genet; 1997 Sep; 17(1):20. PubMed ID: 9288092
[No Abstract] [Full Text] [Related]
36. Is genetics research "minimal risk".
Merz JF
IRB; 1996; 18(6):7-8. PubMed ID: 11654745
[No Abstract] [Full Text] [Related]
37. International Workshop on Legal Aspects of the Human Genome Project (Bilbao, 24-26 May 1993) adopts Bilbao Declaration.
Int Dig Health Legis; 1994; 45(2):234-7. PubMed ID: 11659960
[No Abstract] [Full Text] [Related]
38. Ethical principles of biomedical research on human subjects: their application and limitations in Latin America and the Caribbean.
Serrano LaVertu D; Linares AM
Bull Pan Am Health Organ; 1990; 24(4):469-79. PubMed ID: 2073561
[TBL] [Abstract][Full Text] [Related]
39. WHO's bioethics code likely to stir debate.
Butler D
Nature; 1999 Mar; 398(6724):179. PubMed ID: 10094031
[No Abstract] [Full Text] [Related]
40. Two ethical approaches to research on human beings.
O'Rourke KD
Health Prog; 1988 Oct; 69(8):48-51, 58. PubMed ID: 10290386
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
