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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Bibliografiske detaljer
Udgivet i: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
Format: Artigo
Sprog:Inglês
Udgivet: Future Medicine Ltd 2019
Fag:
Perspective
Online adgang: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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