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Items: 1 to 20 of 656

1.

Returning genetic research results to individuals: points-to-consider.

Renegar G, Webster CJ, Stuerzebecher S, Harty L, Ide SE, Balkite B, Rogalski-Salter TA, Cohen N, Spear BB, Barnes DM, Brazell C.

Bioethics. 2006 Feb;20(1):24-36. Review.

PMID:
16680905
2.

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 May-Aug;19(3-4):1-13. No abstract available.

PMID:
11656943
3.

Family consent and the pursuit of better medicines through genetic research.

Renegar G, Rieser P, Manasco P.

J Contin Educ Health Prof. 2001 Fall;21(4):265-70.

PMID:
11803771
4.

Governing population genomics: law, bioethics, and biopolitics in three case studies.

Winickoff DE.

Jurimetrics. 2003 Winter;43(2):187-228.

PMID:
15156881
5.

Ethical genetic research on human subjects.

Harris J.

Jurimetrics. 1999 Fall;40:77-91.

PMID:
16285118
6.

Property rights in genetic information.

Spinello RA.

Ethics Inf Technol. 2004;6(1):29-42.

PMID:
16969959
7.

National Bioethics Advisory Commission proposed charter; request for comments.

U.S. Office of Science and Technology Policy.

Fed Regist. 1994 Aug 12;59(155):41584-6. No abstract available.

PMID:
11656330
8.

Privacy issues in second stage genomics.

Robertson JA.

Jurimetrics. 1999 Fall;40:59-76.

PMID:
14621715
9.

A legal duty to disclose individual research findings to research subjects?

Gordon MP.

Food Drug Law J. 2009;64(1):225-60.

PMID:
19998747
10.

Privacy and policy for genetic research.

DeCew JW.

Ethics Inf Technol. 2004;6(1):5-14.

PMID:
16969957
11.

Genetic research and ethics.

Great Britain. Advisory Committee on Genetic Testing.

Bull Med Ethics. 1999 Feb;No. 145:21-4. No abstract available.

PMID:
11657252
13.

Participation in pedigree studies and the risk of impeded access to health insurance.

Kass NE.

IRB. 1993 Sep-Oct;15(5):7-10. No abstract available.

PMID:
11659704
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16.

Handling ethical, legal and social issues in birth cohort studies involving genetic research: responses from studies in six countries.

Ries NM, LeGrandeur J, Caulfield T.

BMC Med Ethics. 2010 Mar 23;11:4. doi: 10.1186/1472-6939-11-4. Review.

18.

A biobank management model applicable to biomedical research.

Auray-Blais C, Patenaude J.

BMC Med Ethics. 2006 Apr 6;7:E4.

19.
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