316 related articles for article (PubMed ID: 9736190)
21. Privacy issues in second stage genomics.
Robertson JA
Jurimetrics; 1999; 40():59-76. PubMed ID: 14621715
[TBL] [Abstract][Full Text] [Related]
22. The standard of disclosure in human subject experimentation.
Morin K
J Leg Med; 1998 Jun; 19(2):157-221. PubMed ID: 9658739
[No Abstract] [Full Text] [Related]
23. Monetary inducement to research participation.
Palmer WE
Pharos Alpha Omega Alpha Honor Med Soc; 1985; 48(1):26-30. PubMed ID: 3975268
[No Abstract] [Full Text] [Related]
24. Dangerous intersections.
Korn D
Issues Sci Technol; 1996; 13(1):55-62. PubMed ID: 11654761
[No Abstract] [Full Text] [Related]
25. Ethical principles governing research in child and adolescent psychiatry.
Munir K; Earls F
J Am Acad Child Adolesc Psychiatry; 1992 May; 31(3):408-14. PubMed ID: 1592771
[TBL] [Abstract][Full Text] [Related]
26. Response to open peer commentaries on "assessing the remedy: the case for contracts in clinical trials".
Edwards SJ
Am J Bioeth; 2011 Apr; 11(4):W1-3. PubMed ID: 21480062
[No Abstract] [Full Text] [Related]
27. DNA gatherers hit a snag: the tribes don't trust them.
Harmon A
N Y Times Web; 2006 Dec; ():A1, A38. PubMed ID: 17167865
[No Abstract] [Full Text] [Related]
28. Biobanks: too long to wait for consent.
Brothers KB; Clayton EW
Science; 2009 Nov; 326(5954):798; author reply 799. PubMed ID: 19892963
[No Abstract] [Full Text] [Related]
29. Structuring the review of human genetics protocols, Part II: diagnostic and screening studies.
Glass KC; Weijer C; Lemmens T; Palmour RM; Shapiro SH
IRB; 1997; 19(3-4):1-13. PubMed ID: 11656943
[No Abstract] [Full Text] [Related]
30. Genetics. U.S. hospital launches large biobank of children's DNA.
Kaiser J
Science; 2006 Jun; 312(5780):1584-5. PubMed ID: 16778028
[No Abstract] [Full Text] [Related]
31. Research ethics. Children and population biobanks.
Gurwitz D; Fortier I; Lunshof JE; Knoppers BM
Science; 2009 Aug; 325(5942):818-9. PubMed ID: 19679798
[No Abstract] [Full Text] [Related]
32. Do you understand?: an ethical assessment of researchers' description of the consenting process.
Titus SL; Keane MA
J Clin Ethics; 1996; 7(1):60-8. PubMed ID: 8790700
[No Abstract] [Full Text] [Related]
33. Breast cancer, the genetic "quick fix," and the Jewish community. Ethical, legal, and social challenges.
Rothenberg KH
Health Matrix Clevel; 1997; 7(1):97-124. PubMed ID: 10167180
[No Abstract] [Full Text] [Related]
34. Informed consent: an overview.
Schultz EA
CRNA; 1998 Feb; 9(1):2-9. PubMed ID: 9624941
[TBL] [Abstract][Full Text] [Related]
35. The biological limits on autonomy.
Morison RS
Hastings Cent Rep; 1984 Oct; 14(5):43-9. PubMed ID: 6500919
[TBL] [Abstract][Full Text] [Related]
36. Recommendation No. R (97) 5 of the Committee of Ministers to member states on the protection of medical data.
Council of Europe
Int Dig Health Legis; 1998; 49(3):502-8. PubMed ID: 11657540
[No Abstract] [Full Text] [Related]
37. Biobanks: questioning distinctions.
Hansson MG; Maschke KJ
Science; 2009 Nov; 326(5954):797; author reply 799. PubMed ID: 19892960
[No Abstract] [Full Text] [Related]
38. Informed consent in research and practice. Similarities and differences.
Levine RJ
Arch Intern Med; 1983 Jun; 143(6):1229-31. PubMed ID: 6860050
[No Abstract] [Full Text] [Related]
39. The right to withdraw consent to research on biobank samples.
Helgesson G; Johnsson L
Med Health Care Philos; 2005; 8(3):315-21. PubMed ID: 16283494
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
