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This volume presents the ethical implications of risk information as related to genetics and other health data for policy decisions at clinical, research and societal levels. It will be of great interest to students and scholars of theoretical and clinical medical ethics, medical sociology, risk communication and ethics of risk.
Ulrik Kihlbom is Associate Professor in Medical Ethics at Uppsala University.
Mats G. Hansson is Senior Professor of Biomedical Ethics and Director of The Centre for Research Ethics & Bioethics (CRB) at Uppsala University.
Silke Schicktanz is Full Professor of Cultural and Ethical Studies of Biomedicine at University Medical Center Göttingen.
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