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Volumn 32, Issue 12, 2006, Pages 690-692
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Genetic testing without consent: The implications of the new Human Tissue Act 2004
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Author keywords
[No Author keywords available]
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Indexed keywords
ANTINEOPLASTIC AGENT;
ARTICLE;
CANCER GENETICS;
CANCER RISK;
CLINICAL GENETICS;
CLINICAL PRACTICE;
COLORECTAL CANCER;
DIAGNOSTIC ACCURACY;
DNA DETERMINATION;
GENE MUTATION;
GENETIC IDENTIFICATION;
GENETIC SCREENING;
HUMAN;
HUMAN IMMUNODEFICIENCY VIRUS INFECTION;
HUMAN RIGHTS;
HYSTERECTOMY;
INFORMATION DISSEMINATION;
INFORMED CONSENT;
MEDICOLEGAL ASPECT;
NATIONAL HEALTH SERVICE;
PRACTICE GUIDELINE;
PREDICTION;
PROFESSIONAL MISCONDUCT;
RISK MANAGEMENT;
TISSUE PRESERVATION;
TISSUE SECTION;
UNITED KINGDOM;
UTERUS CANCER;
ACCESS TO INFORMATION;
DISCLOSURE;
ETHICS, MEDICAL;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC PRIVACY;
GENETIC SCREENING;
GREAT BRITAIN;
HUMANS;
LEGISLATION, MEDICAL;
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EID: 33845796058
PISSN: 03066800
EISSN: None
Source Type: Journal
DOI: 10.1136/jme.2005.013631 Document Type: Article |
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Times cited : (15)
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References (9)
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