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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Sparad:
Bibliografiska uppgifter
I publikationen:Per Med
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Future Medicine Ltd 2019
Ämnen:
Perspective
Länkar: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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