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Table of contents (17 papers)
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Introduction: The New Genetics: From Research into Health Care — Social and Ethical Implications for Users and Providers
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Opening Address
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The Provision of the New Genetics: In Whose Best Interest?
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Providing the New Genetics in Primary Care: Problems and Perspectives
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Can the Implementation of New Genetic Tests Be Safeguarded by Consensus Policy Recommendations?
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Critiques on the Provision of the New Genetics: Pros und Cons from Consumer and Provider Perspectives
Editors and Affiliations
Bibliographic Information
Book Title: The New Genetics: From Research into Health Care
Book Subtitle: Social and Ethical Implications for Users and Providers
Editors: Irmgard Nippert, Heidemarie Neitzel, Gerhard Wolff
DOI: https://doi.org/10.1007/978-3-642-58486-2
Publisher: Springer Berlin, Heidelberg
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eBook Packages: Springer Book Archive
Copyright Information: Springer-Verlag Berlin Heidelberg 1999
Softcover ISBN: 978-3-540-65920-4Published: 15 July 1999
eBook ISBN: 978-3-642-58486-2Published: 06 December 2012
Edition Number: 1
Number of Pages: X, 169
Number of Illustrations: 13 b/w illustrations
Topics: Human Genetics, Theory of Medicine/Bioethics, Anthropology, Molecular Medicine