In this book, first published in 2007, bioethics scholars examine the ethical, legal and social questions raised by human genetic databases.
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Matti Häyry is Professor of Bioethics and Philosophy of Law at the University of Manchester.
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Paperback. Zustand: new. Paperback. The Medical Biobank of Umea 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. Human genetic databases raise many ethical, legal and social questions. In this book, first published in 2007, bioethics scholars examine whether existing ethical frameworks and social policies adequately reflect people's concerns, and how these frameworks and policies may need to change in light of new scientific and technological developments. This item is printed on demand. Shipping may be from multiple locations in the US or from the UK, depending on stock availability. Bestandsnummer des Verkäufers 9781107652576
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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. . . . . Bestandsnummer des Verkäufers V9781107652576
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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. Bestandsnummer des Verkäufers V9781107652576
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