Abstract
Abstract:This article examines ethical issues debated in Iceland concerning population genetic research, specifically methods of collecting biosamples and ways to return clinically relevant results to participants. Also discussed are scientific research in the health sector, a bill on surrogacy, and a policy on consent for organ donation.
Publisher
Cambridge University Press (CUP)
Subject
Health Policy,Issues, ethics and legal aspects,Health (social science)
Cited by
3 articles.
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