Consent for genetics studies among clinical trial participants: findings from Action for Health in Diabetes (Look AHEAD)

Background Increasingly, genetic specimens are collected to expand the value of clinical trials through study of genetic effects on disease incidence, progression or response to interventions. Purpose and methods We describe the experience obtaining IRB-approved DNA consent forms across the 19 insti...

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Veröffentlicht in:Clinical trials (London, England) England), 2006-10, Vol.3 (5), p.443-456
Hauptverfasser: Espeland, M A, Dotson, K, Jaramillo, S A, Kahn, S E, Harrison, B, Montez, M, Foreyt, J P, Montgomery, B, Knowler, W C
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Sprache:eng
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