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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Dades bibliogràfiques
Publicat a:Per Med
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Future Medicine Ltd 2019
Matèries:
Perspective
Accés en línia: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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