A proposal for a model of informed consent for the collection, storage and use of biological materials for research purposes

Author:

Porteri Corinna,Borry Pascal

Publisher

Elsevier BV

Subject

General Medicine

Reference22 articles.

1. Monitoring ethical, legal and social issues in developing population genetic databases;Austin;Genet Med,2003

2. Godard B, Schmidtke J, Cassiman JJ, Aymé S. Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issue, ownership, return of benefits. A Professional Perspective. EUROGAPP PROJECT 1999–2000. ESHG 1; November 2002.

3. Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research;Hoeyer;Scand J Public Health,2004

4. The ethics of research using biobanks. Reason to question the importance attributed to informed consent;Hoeyer;Arch Intern Med,2005

5. Science is really needed—that's all I know: informed consent and the non-verbal practices of collecting blood for genetic research in Northen Sweden;Hoeyer;New Genet Soc,2003

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