Public participation in genetic databases: crossing the boundaries between biobanks and forensic DNA databases through the principle of solidarity
Author:
Publisher
BMJ
Subject
Health Policy,Arts and Humanities (miscellaneous),Issues, ethics and legal aspects,Health (social science)
Reference26 articles.
1. Genomics for public health improvement: relevant international ethical and policy issues around genome-wide association studies and biobanks;Pang;Public Health Genomics,2013
2. Publics and biobanks: pan-European diversity and the challenge of responsible innovation;Gaskell;Eur J Hum Genet,2013
3. Forensic DNA databases: genetic testing as a societal choice;Patyn;J Med Ethics,2010
4. Forensic genetics and ethical, legal and social implications beyond the clinic;Cho;Nat Genet,2004
5. The retention of forensic samples: a socio-ethical evaluation of current practices in the EU;Van Camp;J Med Ethics,2008
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