9781107652576 - The Ethics and Governance of Human Genetic Databases: European Perspectives di Häyry, Matti (15 risultati)

Condizione: New.

Condizione: New. In.

Paperback. Condizione: New.

Condizione: 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. . . . .

Condizione: New. pp. 296.

Condizione: 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.

Taschenbuch. Condizione: 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.

Paperback. Condizione: 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.

Paperback. Condizione: Brand New. 1st edition. 283 pages. 8.75x5.75x0.50 inches. In Stock. This item is printed on demand.

Paperback / softback. Condizione: New. This item is printed on demand. New copy - Usually dispatched within 5-9 working days.

Condizione: New. Print on Demand pp. 296 23:B&W 6 x 9 in or 229 x 152 mm Perfect Bound on White w/Gloss Lam.

Condizione: New. PRINT ON DEMAND pp. 296.

Paperback. Condizione: 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 our UK warehouse or from our Australian or US warehouses, depending on stock availability.

Condizione: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. 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 .

Paperback. Condizione: 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 our Sydney, NSW warehouse or from our UK or US warehouse, depending on stock availability.