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3. [Ethical problems presented by collections of biological material and associated data: "biobanks", "bioethics"]. France. Comite consultatif national d'ethique pour les sciences de la vie et de la sante J Int Bioethique; 2005; 16(3-4):141-51. PubMed ID: 17058808 [No Abstract] [Full Text] [Related]
4. "Broad" consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose. Petrini C Soc Sci Med; 2010 Jan; 70(2):217-20. PubMed ID: 19853341 [TBL] [Abstract][Full Text] [Related]
5. Genotyping in clinical trials: towards a principle of informed request. Sass HM J Med Philos; 1998 Jun; 23(3):288-96. PubMed ID: 9736190 [TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Biobanks and the new law. Renew informed consent with moderation for tests which are to be used for new purposes]. Eriksson S Lakartidningen; 2003 Dec; 100(49):4106-9. PubMed ID: 14717077 [No Abstract] [Full Text] [Related]
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11. Biobanks. Population databases boom, from Iceland to the U.S. Kaiser J Science; 2002 Nov; 298(5596):1158-61. PubMed ID: 12424349 [No Abstract] [Full Text] [Related]
14. Alternative consent models for biobanks: the new Spanish law on biomedical research. da Rocha AC; Seoane JA Bioethics; 2008 Sep; 22(8):440-7. PubMed ID: 18644013 [TBL] [Abstract][Full Text] [Related]
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