DNA databanks and consent: A suggested policy option involving an authorization model-Reference-Cited by-同舟云学术

DNA databanks and consent: A suggested policy option involving an authorization model

Published:2003-01-03 Issue:1 Volume:4 Page:
ISSN:1472-6939
Container-title:BMC Medical Ethics
language:en
Short-container-title:BMC Med Ethics

Author:

Caulfield Timothy,Upshur Ross EG,Daar Abdallah

Publisher

Springer Science and Business Media LLC

Subject

Health Policy,Health(social science),Issues, ethics and legal aspects

Link

http://link.springer.com/content/pdf/10.1186/1472-6939-4-1.pdf

Reference26 articles.

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3. Weijer C, Emanuel EJ: Ethics. Protecting communities in biomedical research. Science. 2000, 289: 1142-1144. 10.1126/science.289.5482.1142.

4. Greely HT: Human genome diversity: what about the other human genome project?. Nat Rev Genet. 2001, 2: 222-227. 10.1038/35056071.

5. National Bioethics Advisory Commission: Research Involving Human Biological Material: Ethical Issues and Policy Guidance. Rockville: US Government Printing Office. 1999

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