Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Hardcover. Zustand: Very Good. Bumped edges Slight scratches to cover Appears unread, may have minor damage from transit/storage. Next day dispatch from the UK (Mon-Fri). Please contact us with any queries.
Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Madrid. Revista. Rústica 14,5x21. 169 pp.
Verlag: Thela Thesis 1999, 1999
ISBN 10: 9051704852 ISBN 13: 9789051704853
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409 p. Paperback.
Verlag: Campus Verlag, 2015
ISBN 10: 3593501902 ISBN 13: 9783593501901
Anbieter: moluna, Greven, Deutschland
Zustand: New. Nach wie vor sind wir weit entfernt davon, psychische Phaenomene wirklich zu verstehen. Vielfach geraet bei der Behandlung der Patient als ganzer Mensch aus dem Blickfeld, und psychische Stoerungen werden auf hirnphysiologische Phaenomene reduziert. In einer .
Verlag: Berghahn Books, Incorporated, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Verlag: Berghahn Books, Incorporated, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Verlag: Berghahn Books, Incorporated, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Hardback. Zustand: New. New copy - Usually dispatched within 4 working days. This workbook for practitioners and students deals with the ethical implications of clinical genetics, as well as ethical issues involved in genetic screening, the research of populations, and the use of genetic information for access to insurance and the workplace. Suggestions for activities and qu.
Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Zustand: New.
Verlag: Berghahn Books, Incorporated, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
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Verlag: BERGHAHN BOOKS INC, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
Anbieter: moluna, Greven, Deutschland
Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. This workbook for practitioners and students deals with the ethical implications of clinical genetics, as well as ethical issues involved in genetic screening, the research of populations, and the use of genetic information for access to insurance and the w.
Verlag: Berghahn Books, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Genetic information plays an increasingly important role in ourlives. As a result of the Human Genome Project, knowledge ofthe genetic basis of various diseases is growing, withimportant consequences for the role of genetics in clinicalpractice, health care systems and for society at large. In theclinical setting genetic testing may result in a better insightinto susceptibility for inheritable diseases, not only before orafter birth, but also at later stages in life. Besides prenataltesting and pre-conceptional testing, predictive testing hasresulted in new possibilities for the early detection, treatmentand prevention of inheritable diseases.However, not all inheritable diseases that can be predicted onthe basis of genetic information can be treated or cured.Should we offer genetic tests to people for untreatablediseases Should we test every individual who wants to knowhis or her genetic status Should we inform family membersabout the results of genetic tests of individuals, even whenthere are no possibilities for treatment What, in such cases,is the role of the 'right-not-to-know' Should we informfamily members when there is only an increased risk of adisease This book deals with the ethical issues of clinicalgenetics, as well as ethical issues that arise in geneticscreening, the research of populations, and the use of geneticinformation for access to insurance and the workplace.
Verlag: Berghahn Books, Incorporated, Herndon, 2003
ISBN 10: 1571816003 ISBN 13: 9781571816009
Anbieter: AussieBookSeller, Truganina, VIC, Australien
Hardcover. Zustand: new. Hardcover. Genetic information plays an increasingly important role in ourlives. As a result of the Human Genome Project, knowledge ofthe genetic basis of various diseases is growing, withimportant consequences for the role of genetics in clinicalpractice, health care systems and for society at large. In theclinical setting genetic testing may result in a better insightinto susceptibility for inheritable diseases, not only before orafter birth, but also at later stages in life. Besides prenataltesting and pre-conceptional testing, predictive testing hasresulted in new possibilities for the early detection, treatmentand prevention of inheritable diseases.However, not all inheritable diseases that can be predicted onthe basis of genetic information can be treated or cured.Should we offer genetic tests to people for untreatablediseases? Should we test every individual who wants to knowhis or her genetic status? Should we inform family membersabout the results of genetic tests of individuals, even whenthere are no possibilities for treatment? What, in such cases,is the role of the "right-not-to-know"? Should we informfamily members when there is only an increased risk of adisease? This book deals with the ethical issues of clinicalgenetics, as well as ethical issues that arise in geneticscreening, the research of populations, and the use of geneticinformation for access to insurance and the workplace. This book deals with the ethical issues that arise in the process of genetic screening, the research of population and the use of genetic information for access to insurance and the workplace. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.