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Published by Cambridge University Press, 2003
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Published by Cambridge University Press, 2003
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Published by LAP LAMBERT Academic Publishing, 2012
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Taschenbuch. Condition: Neu. Genetic Information - Values and Rights | The Morality of Presymptomatic Genetic Testing | Niklas Juth | Taschenbuch | 484 S. | Englisch | 2012 | LAP LAMBERT Academic Publishing | EAN 9783846588819 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.
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Published by Cambridge University Press, 2007
ISBN 10: 0521054508 ISBN 13: 9780521054508
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Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. The genetic information that is available to insurance companies has often been regulated to avoid certain ethical difficulties. However, regulation may not be the solution, argue the authors, and suggest instead the resurrection of collectively funded publ.
Language: English
Published by LAP LAMBERT Academic Publishing Feb 2012, 2012
ISBN 10: 3846588814 ISBN 13: 9783846588819
Seller: BuchWeltWeit Ludwig Meier e.K., Bergisch Gladbach, Germany
Taschenbuch. Condition: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -This book discusses the moral concerns due to the increasing possibilities to predict individuals health on the basis of genetic testing. To what extent should such testing be performed Which parties should be allowed to gain access to the results of such testing The scope and limits of patients right to know and not know are presented. It is also argued that patients value of presymptomatic genetic testing ultimately rests on autonomy and subjective well-being. Moreover, a conception of autonomy is developed, which is useful to analyse the novel idea in this area that autonomy is a value that should be promoted. Regarding the question of blood relatives rights to genetic information, it is argued that we should generally leave the decision to inform relatives to the tested person. The idea that genetic information belongs to a new paradigm of medical information that is communal in its nature is criticized. Broader societal questions regarding e.g. insurance companies right to genetic information are also discussed. It is argued that the development of genetics strengthens the need for and defence of a comprehensive welfare state. 484 pp. Englisch.
Language: English
Published by LAP LAMBERT Academic Publishing, 2012
ISBN 10: 3846588814 ISBN 13: 9783846588819
Seller: moluna, Greven, Germany
Condition: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Juth NiklasNiklas Juth is a senior lecturer and researcher in medical ethics at Karolinska Institutet. His main research interests are in ethics and bioethics, genethics, and the intersection between political philosophy and medical .