Consent for clinical genome sequencing: considerations from the Clinical Sequencing Exploratory Research Consortium

Implementing genome and exome sequencing in clinical practice presents challenges, including obtaining meaningful informed consent. Consent may be challenging due to test limitations such as uncertainties associated with test results and interpretation, complexity created by the potential for additi...

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Detalhes bibliográficos
Publicado no:Per Med
Main Authors: Yu, Joon-Ho, Appelbaum, Paul S, Brothers, Kyle B, Joffe, Steven, Kauffman, Tia L, Koenig, Barbara A, Prince, Anya ER, Scollon, Sarah, Wolf, Susan M, Bernhardt, Barbara A, Wilfond, Benjamin S
Formato: Artigo
Idioma:Inglês
Publicado em: Future Medicine Ltd 2019
Assuntos:
Perspective
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6681646/
https://ncbi.nlm.nih.gov/pubmed/31313633
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2217/pme-2018-0076
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