Sprache: Englisch
Verlag: Cambridge University Press, 2007
ISBN 10: 0521856620 ISBN 13: 9780521856621
Anbieter: Anybook.com, Lincoln, Vereinigtes Königreich
EUR 13,45
Anzahl: 1 verfügbar
In den WarenkorbZustand: Fair. This is an ex-library book and may have the usual library/used-book markings inside.This book has hardback covers. Clean from markings. In fair condition, suitable as a study copy. No dust jacket. Please note the Image in this listing is a stock photo and may not match the covers of the actual item,700grams, ISBN:9780521856621.
Sprache: Englisch
Verlag: Cambridge University Press, 2007
ISBN 10: 0521856620 ISBN 13: 9780521856621
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 127,58
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Anbieter: Revaluation Books, Exeter, Vereinigtes Königreich
EUR 180,49
Anzahl: 2 verfügbar
In den WarenkorbHardcover. Zustand: Brand New. 283 pages. 9.25x6.50x0.75 inches. In Stock.
Sprache: Englisch
Verlag: Cambridge University Press, 2007
ISBN 10: 0521856620 ISBN 13: 9780521856621
Anbieter: Vulkaneifel Bücher, Birgel, Deutschland
Zustand: Sehr gut. kleine Lagerspuren am Buch, Inhalt einwandfrei und ungelesen Sprache: Englisch Gewicht in Gramm: 620.
Sprache: Englisch
Verlag: Cambridge University Press, 2007
ISBN 10: 0521856620 ISBN 13: 9780521856621
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Buch. Zustand: Neu. Druck auf Anfrage Neuware - Printed after ordering - The Medical Biobank of Umeå in Sweden, deCODE's Health Sector Database in Iceland, the Estonian Genome Project and the UK Biobank contain health data and genetic data from large populations. Some include genealogical or lifestyle information. They are resources for research in human genetics and medicine, exploring interaction between genes, lifestyle, environmental factors and health and diseases. The collection, storage and use of this data raise ethical, legal and social issues. In this book, bioethics scholars examine whether existing ethical frameworks and social policies reflect people's concerns, and how they may need to change in light of new scientific and technological developments. The ethical issues of social justice, genetic discrimination, informational privacy, trust in science and consent to participation in database research are analyzed, whilst an empirical survey, conducted in the four countries, demonstrates public views of privacy and related moral values in the context of human genetic databases.
Sprache: Englisch
Verlag: Cambridge University Press, 2007
ISBN 10: 0521856620 ISBN 13: 9780521856621
Anbieter: Kennys Bookstore, Olney, MD, USA
EUR 242,65
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In this book, first published in 2007, bioethics scholars examine the ethical, legal and social questions raised by human genetic databases. Series Editor(s): McCall Smith, Alexander. Series: Cambridge Law, Medicine & Ethics. Num Pages: 296 pages, black & white illustrations. BIC Classification: 1DBKE; 1DBKW; LNTM; MBDC. Category: (P) Professional & Vocational. Dimension: 238 x 160 x 25. Weight in Grams: 652. . 2007. hardcover. . . . . Books ship from the US and Ireland.