Genetic databases : socio-ethical issues in the collection and use of DNA /
Genetic Databases offers a timely analysis of the underlying tensions, contradictions and limitations of the current regulatory frameworks for and policy debates about genetic databases.
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| Other Authors: | , |
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| Format: | Electronic eBook |
| Language: | English |
| Published: |
London ; New York :
Routledge,
2004.
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| Subjects: | |
| Online Access: | CONNECT |
Table of Contents:
- Introduction : public participation in genetic databases / Richard Tutton and Oonagh Corrigan
- Person, property and gift : exploring languages of tissue donation to biomedical research / Richard Tutton
- Blood donation for genetic research : what can we learn from donors' narratives? / Helen Busby
- Levels and styles of participation in genetic databases : a case study of the North Cumbria Community Genetics Project / Erica Haimes and Michael Whong-Barr
- Informed consent : the contradictory ethical safeguards in pharmacogenetics / Oonagh Corrigan
- Ambiguous gifts : public anxiety, informed consent and biobanks / Klaus Hoeyer
- Abandoning informed consent : the case of genetic research in population collections / Jane Kaye
- Children's participation in genetic epidemiology : consent and control / Emma Williamson [and others]
- 'Public consent' or 'scientific citizenship'? What counts as public participation in population-based DNA collections? / Sue Weldon
- Tissue collection and the pharmaceutical industry : investigating corporate biobanks / Graham Lewis.
