Sprache: Englisch
Verlag: Cambridge University Press, 2013
ISBN 10: 110765257X ISBN 13: 9781107652576
Anbieter: Ria Christie Collections, Uxbridge, Vereinigtes Königreich
EUR 44,26
Anzahl: Mehr als 20 verfügbar
In den WarenkorbZustand: New. In.
Sprache: Englisch
Verlag: Cambridge University Press, 2013
ISBN 10: 110765257X ISBN 13: 9781107652576
Anbieter: Kennys Bookstore, Olney, MD, USA
Zustand: New. In this book, first published in 2007, bioethics scholars examine the ethical, legal and social questions raised by human genetic databases. Series: Cambridge Law, Medicine & Ethics. Num Pages: 296 pages, black & white illustrations. BIC Classification: LNTM; MBQ. Category: (P) Professional & Vocational. Dimension: 228 x 152 x 16. . . 2013. Paperback. . . . . Books ship from the US and Ireland.
Sprache: Englisch
Verlag: Cambridge University Press, 2013
ISBN 10: 110765257X ISBN 13: 9781107652576
Anbieter: AHA-BUCH GmbH, Einbeck, Deutschland
Taschenbuch. 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, first published in 2007, 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.