Isbn: 9781107429796 - the right to know and the right not to know: genetic privacy and responsibility (cambridge bioethics and law) (8 Ergebnisse)

Paperback. Zustand: Very Good. No Jacket. Former library book; May have limited writing in cover pages. Pages are unmarked. ~ ThriftBooks: Read More, Spend Less.

Paperback. Zustand: As New. 2nd edition. Very good condition unread paperback with minimal wear. Contents are clean and bright throughout with no markings.

Paperback. Zustand: As New. 2nd edition. Very good condition unread paperback with minimal wear. Contents are clean and bright throughout with no markings.

Zustand: Good. 2nd Edition. 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.

Zustand: New. In English.

Paperback. Zustand: Brand New. 2nd edition. 240 pages. 9.00x6.00x0.50 inches. In Stock.

Zustand: New. This book re-examines privacy in a world where genome sequencing is cheap, databases can be large, and access rights are hidden. Editor(s): Chadwick, Professor Ruth; Levitt, Mairi; Shickle, Darren. Series: Cambridge Bioethics and Law. Num Pages: 228 pages, 1 b/w illus. BIC Classification: LNTM; MBDC; PSAD. Category: (P) Professional & Vocational; (U) Tertiary Education (US: College). Dimension: 226 x 155 x 13. Weight in Grams: 346. . 2014. 2nd Edition. Paperback. . . . . Books ship from the US and Ireland.…

Taschenbuch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - The privacy concerns discussed in the 1990s in relation to the New Genetics failed to anticipate the relevant issues for individuals, families, geneticists and society. Consumers, for example, can now buy their personal genetic information and share it online. The challenges facing genetic privacy have evolved as new biotechnologies have developed, and personal privacy is increasingly challenged by the irrepressible flow of electronic data between the personal and public spheres and by surveillance for terrorism and security risks. This book considers the right to know and the right not to know about your own and others' genomes. It discusses new privacy concerns and developments in ethical thinking, with the greater emphasis on solidarity and equity. The multidisciplinary approach covers current topics such as biobanks and forensic databases, DIY testing, group rights and accountability, the food we eat and the role of the press and the new digital media.…