290 related articles for article (PubMed ID: 7777074)
1. Ethical implications of the Human Genome Diversity Project.
McPherson EC
Nursingconnections; 1995; 8(1):36-43. PubMed ID: 7777074
[No Abstract] [Full Text] [Related]
2. Scientific imperialism or service to humanity? The complexities of the Human Genome Diversity Project.
Creskoff K
Princet J Bioeth; 1998; 1(1):6-22. PubMed ID: 11657339
[No Abstract] [Full Text] [Related]
3. The Human Genome Diversity Project: medical benefits versus ethical concerns.
Wallace RW
Mol Med Today; 1998 Feb; 4(2):59-62. PubMed ID: 9547791
[TBL] [Abstract][Full Text] [Related]
4. Governing population genomics: law, bioethics, and biopolitics in three case studies.
Winickoff DE
Jurimetrics; 2003; 43(2):187-228. PubMed ID: 15156881
[TBL] [Abstract][Full Text] [Related]
5. International guidelines for ethical review of epidemiological studies.
Law Med Health Care; 1991; 19(3-4):247-58. PubMed ID: 1779694
[No Abstract] [Full Text] [Related]
6. The Human Genome Diversity Project: ethical problems and solutions.
Resnik DB
Politics Life Sci; 1999 Mar; 18(1):15-23. PubMed ID: 11660815
[No Abstract] [Full Text] [Related]
7. Consent, ethics, and community.
Loewy EH
J Clin Ethics; 1992; 3(3):224-8. PubMed ID: 1392045
[No Abstract] [Full Text] [Related]
8. Informed consent in medical research. Doctors are arrogant to think they need to debate issue of patient consent.
Bratt DE
BMJ; 1997 May; 314(7092):1477. PubMed ID: 9167569
[No Abstract] [Full Text] [Related]
9. 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]
10. HUGO approves ethics code for genomics.
Dickson D
Nature; 1996 Mar; 380(6572):279. PubMed ID: 8598922
[No Abstract] [Full Text] [Related]
11. Protecting communities in research: philosophical and pragmatic challenges.
Weijer C
Camb Q Healthc Ethics; 1999; 8(4):501-13. PubMed ID: 10513308
[No Abstract] [Full Text] [Related]
12. The Human Genome Diversity Project and its implications for indigenous peoples.
Harry D
Genewatch; 1996 Oct; 10(2-3):8-9. PubMed ID: 11660352
[No Abstract] [Full Text] [Related]
13. Ethical imperialism and informed consent.
Newton LH
IRB; 1990; 12(3):10-1. PubMed ID: 11659442
[No Abstract] [Full Text] [Related]
14. Tribal groups attack ethics of genome diversity project.
Macilwain C
Nature; 1996 Sep; 383(6597):208. PubMed ID: 8805684
[No Abstract] [Full Text] [Related]
15. Genetics, ethics, and human values: human genome mapping, genetic screening and gene therapy.
Miller J
NCBHR Commun; 1990; 1(1):11-3. PubMed ID: 11660184
[No Abstract] [Full Text] [Related]
16. Proxy consent and a national DNA databank: an unethical and discriminatory combination.
Baumann TK
Iowa Law Rev; 2001 Jan; 86(2):667-701. PubMed ID: 16184651
[No Abstract] [Full Text] [Related]
17. Ethical issues in genetic research: disclosure and informed consent.
Reilly PR; Boshar MF; Holtzman SH
Nat Genet; 1997 Jan; 15(1):16-20. PubMed ID: 8988163
[TBL] [Abstract][Full Text] [Related]
18. Dangerous intersections.
Korn D
Issues Sci Technol; 1996; 13(1):55-62. PubMed ID: 11654761
[No Abstract] [Full Text] [Related]
19. Circumcision revisited.
Kessel R
Hastings Cent Rep; 1997; 27(2):4; author reply 5. PubMed ID: 9131342
[No Abstract] [Full Text] [Related]
20. Proposed model ethical protocol for collecting DNA samples.
Weiss KM; Cavalli-Sforza LL; Dunston GM; Feldman M; Greely HT; Kidd KK; King M; Moore JA; Szathmary E; Twinn CM;
Houst Law Rev; 1997; 33(5):1431-74. PubMed ID: 12627556
[No Abstract] [Full Text] [Related]
[Next] [New Search]
