Patient perspectives on group benefits and harms in genetic research

Public Health Genomics

Volumn 14, Issue 3, 2011, Pages 135-142

  Goldenberg, A J ^a   Hull, S C ^b   Wilfond, B S ^c,d   Sharp, R R ^a,e  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

^c UNIVERSITY OF WASHINGTON SCHOOL OF MEDICINE   (United States)

^d UNIVERSITY OF WASHINGTON   (United States)

^e LERNER RESEARCH INSTITUTE   (United States)

Author keywords

Biorepositories; Community consultation; Ethics; Genetic research; Group harm; Human subjects; Informed consent; Stored tissue

Indexed keywords

BIOMATERIAL; DNA;

ADULT; AGED; ARTICLE; BLOOD SAMPLING; CLINICAL PRACTICE; CLINICAL RESEARCH; COMMUNITY; CONSULTATION; DONOR; ETHICS; FEMALE; GENETICS; HEALTH CARE FACILITY; HEALTH CARE POLICY; HUMAN; HUMAN GENETICS; MAJOR CLINICAL STUDY; MALE; MEDICAL ETHICS; MEDICAL RESEARCH; PATIENT ATTITUDE; PATIENT DECISION MAKING; PRACTICE GUIDELINE; PRIORITY JOURNAL; UNITED STATES;

ATTITUDE; GENETIC RESEARCH; HUMANS; INFORMED CONSENT; PATIENTS; UNITED STATES;

EID: 79956066390     PISSN: 16624246     EISSN: 16628063     Source Type: Journal    
DOI: 10.1159/000317497     Document Type: Article

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