Genetic databases Socio-ethical issues in the collection and use of DNA

Genetic Databases offers a timely analysis of the underlying tensions, contradictions and limitations of the current regulatory frameworks for, and policy debates about, genetic databases. Drawing on original empirical research and theoretical debates in the fields of sociology, anthropology and leg...

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Bibliographische Detailangaben
Hauptverfasser:	Tutton, Richard, Corrigan, Oonagh
Format:	E-Book Buch
Sprache:	Englisch
Veröffentlicht:	London Routledge 2004 Taylor and Francis Taylor & Francis Group
Ausgabe:	1
Schlagworte:	Amino acid sequence Bioinformatics Biotechnology Citizen participation Data processing Databases, Genetic > ethics DNA DNA data banks Genetics Genomics Informed Consent Informed consent (Medical law) Medical ethics New Genetics Nucleotide sequence Sociology of Health and Illness trust icelandic PXE International National DNA Database Non-therapeutic Research UK Medical Research Council UK House issues Informed Consent Procedures Human Genetic Databases Informed Consent Medical Biobank Population Collection socio-ethical Clinical Drug Trials UK Drug Company biobank sector informed Icelandic Health Sector Database Genetic Databases DNA Bank health Estonian Genome Project consent DNA Sample Health Sector Database ALSPAC Study Public Engagement Sensitive Information UK's National Health Service Mother's Questionnaire UK Biobank wellcome Human Biological Material
ISBN:	9780415316798, 0415316790, 9780415316804, 0415316804
Online-Zugang:	Volltext
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