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Long-term trends in public sensitivities about genetic identification: 1973-2002

By Martin. W Bauer

Abstract

Iceland is an appropriate venue for a forum on the implications of genetic databases because the country collects medical data on all of its residents, living and deceased. International contributors to the conference held at the U. of Iceland in summer 2004 address their experiences with such databases and controversies over such issues as informed consent, privacy, genetic property rights, and research and public health use

Topics: QH Natural history
Publisher: University of Iceland Press
Year: 2004
OAI identifier: oai:eprints.lse.ac.uk:9510
Provided by: LSE Research Online
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