Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Paperback. Zustand: Very Good. crisp clean w/light shelfwear/edgewear - may have remainder mark Standard-sized.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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In den WarenkorbPaperback. Zustand: Very Good. The book has been read, but is in excellent condition. Pages are intact and not marred by notes or highlighting. The spine remains undamaged.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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In den WarenkorbSoft cover. Zustand: Very Good. Has some light general reading/shelfwear - otherwise this is a clean, tight copy. Quick dispatch from the UK.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521833140 ISBN 13: 9780521833141
Sprache: Englisch
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hardcover. Zustand: Very Good. No DJ as issued No dust jacket. Very Good hardcover with light shelfwear - NICE! Standard-sized.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: Poverty Hill Books, Mt. Prospect, IL, USA
Paperback. Zustand: New. BRAND NEW, Perfect Shape, No Remainder Mark,Fast Shipping With Online Tracking, International Orders shipped Global Priority Air Mail, All orders handled with care and shipped promptly in secure packaging, we ship Mon-Sat and send shipment confirmation emails. Our customer service is friendly, we answer emails fast, accept returns and work hard to deliver 100% Customer Satisfaction!
Verlag: Cambridge University Press CUP, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: Books Puddle, New York, NY, USA
Zustand: New. pp. 216.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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In den WarenkorbZustand: New. pp. 216.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: Romtrade Corp., STERLING HEIGHTS, MI, USA
Zustand: New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Brand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521833140 ISBN 13: 9780521833141
Sprache: Englisch
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In den WarenkorbOriginal Boards. Zustand: As New. Zustand des Schutzumschlags: No Dust Jacket. First Edition; First Edition. 203 pages. Lacks dustjacket. Stamped damaged on verso title page. Otherwise in new condition with only minor shelfwear. ; Hardcover; Octavo; This book explores the way changes in technology have altered the relationship between ethics and medicine. For some inherited diseases, new genetic testing technologies may provide much more accurate diagnostic and predictive information which raises important questions about consent, confidentiality and use of the information by family members and other third parties. What are the implications of this knowledge for individuals and their families? And for society more widely? How should this new information be used? How do people deal with the choices that new knowledge and technologies offer? Drawing on extensive ethnographic research with families affected by Huntington's Disease, and using perspectives from medical and cultural anthropology, the author explores the huge disparity between the experience of living with the results of genetic testing and the knowledge and expertise which are drawn on to develop policy and clinical services.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: ALLBOOKS1, Direk, SA, Australien
Brand new book. Fast ship. Please provide full street address as we are not able to ship to P O box address.
Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521833140 ISBN 13: 9780521833141
Sprache: Englisch
Cloth. Fine.; 8vo.
Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: Grand Eagle Retail, Bensenville, IL, USA
Paperback. Zustand: new. Paperback. This book explores the way changes in technology have altered the relationship between ethics and medicine. For some inherited diseases, new genetic testing technologies may provide much more accurate diagnostic and predictive information which raises important questions about consent, confidentiality and use of the information by family members and other third parties. What are the implications of this knowledge for individuals and their families? And for society more widely? How should this new information be used? How do people deal with the choices that new knowledge and technologies offer? Drawing on extensive ethnographic research with families affected by Huntington's Disease, and using perspectives from medical and cultural anthropology, the author explores the huge disparity between the experience of living with the results of genetic testing and the knowledge and expertise which are drawn on to develop policy and clinical services. This work explores the way changes in technology have affected the relationship between ethics and medicine, generating new approaches to ethical issues and the implications of medical practice. Drawing on extensive ethnographic research with families affected by Huntington's Disease, Monica Konrad explores the huge disparity between the experience of living with the results of genetic testing and the knowledge and expertise to develop policy, clinical services and support. Shipping may be from multiple locations in the US or from the UK, depending on stock availability.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: Antiquariaat Ovidius, Bredevoort, Niederlande
Zustand: Gebraucht / Used. Fine state. d599e.
Verlag: Cambridge University Press, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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In den WarenkorbZustand: New. In.
Verlag: Cambridge University Press 2005-02-17, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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In den WarenkorbPaperback. Zustand: New.
Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: Antiquariat Bücherwurm Kiel, Kiel, Deutschland
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In den WarenkorbPaperback. Zustand: Brand New. 203 pages. 8.75x5.75x0.50 inches. In Stock.
Verlag: Cambridge University Press, United Kingdom, 2005
ISBN 10: 0521833140 ISBN 13: 9780521833141
Sprache: Englisch
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In den WarenkorbHardcover. Zustand: As New. Brand new hardcover Unread but may have "damaged" stamp on one of the title pages due to cosmetic imperfection such as minor dents on cover or edge of pages or scratches on cover etc.
Verlag: Cambridge University Press, United Kingdom, 2005
ISBN 10: 0521833140 ISBN 13: 9780521833141
Sprache: Englisch
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Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
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In den WarenkorbPaperback. Zustand: new. Paperback. This book explores the way changes in technology have altered the relationship between ethics and medicine. For some inherited diseases, new genetic testing technologies may provide much more accurate diagnostic and predictive information which raises important questions about consent, confidentiality and use of the information by family members and other third parties. What are the implications of this knowledge for individuals and their families? And for society more widely? How should this new information be used? How do people deal with the choices that new knowledge and technologies offer? Drawing on extensive ethnographic research with families affected by Huntington's Disease, and using perspectives from medical and cultural anthropology, the author explores the huge disparity between the experience of living with the results of genetic testing and the knowledge and expertise which are drawn on to develop policy and clinical services. This work explores the way changes in technology have affected the relationship between ethics and medicine, generating new approaches to ethical issues and the implications of medical practice. Drawing on extensive ethnographic research with families affected by Huntington's Disease, Monica Konrad explores the huge disparity between the experience of living with the results of genetic testing and the knowledge and expertise to develop policy, clinical services and support. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
Verlag: Cambridge University Press, Cambridge, 2005
ISBN 10: 0521540666 ISBN 13: 9780521540667
Sprache: Englisch
Anbieter: AussieBookSeller, Truganina, VIC, Australien
Paperback. Zustand: new. Paperback. This book explores the way changes in technology have altered the relationship between ethics and medicine. For some inherited diseases, new genetic testing technologies may provide much more accurate diagnostic and predictive information which raises important questions about consent, confidentiality and use of the information by family members and other third parties. What are the implications of this knowledge for individuals and their families? And for society more widely? How should this new information be used? How do people deal with the choices that new knowledge and technologies offer? Drawing on extensive ethnographic research with families affected by Huntington's Disease, and using perspectives from medical and cultural anthropology, the author explores the huge disparity between the experience of living with the results of genetic testing and the knowledge and expertise which are drawn on to develop policy and clinical services. This work explores the way changes in technology have affected the relationship between ethics and medicine, generating new approaches to ethical issues and the implications of medical practice. Drawing on extensive ethnographic research with families affected by Huntington's Disease, Monica Konrad explores the huge disparity between the experience of living with the results of genetic testing and the knowledge and expertise to develop policy, clinical services and support. Shipping may be from our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.
Verlag: Cambridge University Press, U.S.A., 2005
ISBN 10: 0521833140 ISBN 13: 9780521833141
Sprache: Englisch
Anbieter: RIVERLEE BOOKS, Waltham Cross, HERTS, Vereinigtes Königreich
EUR 80,62
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In den WarenkorbHardcover. Zustand: As New. Brand new hardcover Unread but may have "damaged" stamp on one of the title pages due to cosmetic imperfection such as minor dents on cover or edge of pages or scratches on cover etc.