ISBN: 9780521833141 - narrating the new predictive genetics: ethics, ethnography and science (cambridge studies in society and the life sciences) (8 Ergebnisse)

Zustand: Good. Pages intact with minimal writing/highlighting. The binding may be loose and creased. Dust jackets/supplements are not included. Stock photo provided. Product includes identifying sticker. Better World Books: Buy Books. Do Good.

Hardcover. 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.

Hardcover. 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.

Hardcover. 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.

Zustand: As New. Unread book in perfect condition.

Hardcover. Zustand: Brand New. 203 pages. 9.25x6.25x1.00 inches. In Stock.

Zustand: New. Explores how new techniques in genetic testing have changed the relationship between ethics and medicine. Series: Cambridge Studies in Society & the Life Sciences. Num Pages: 216 pages, 1 b/w illus. BIC Classification: MBDC. Category: (P) Professional & Vocational. Dimension: 228 x 152 x 23. Weight in Grams: 463. . 2005. hardcover. . . . . Books ship from the US and Ireland.…

Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - 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.…