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...

Celý popis

Uloženo v:

Podrobná bibliografie
Hlavní autoři:	Tutton, Richard, Corrigan, Oonagh
Médium:	E-kniha Kniha
Jazyk:	angličtina
Vydáno:	London Routledge 2004 Taylor and Francis Taylor & Francis Group
Vydání:	1
Témata:	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
On-line přístup:	Získat plný text
Tagy:	Přidat tag Žádné tagy, Buďte první, kdo vytvoří štítek k tomuto záznamu!

Buďte první, kdo okomentuje tento záznam!