Reporting incidental findings of genomic disorder-associated copy number variants to unselected biobank participants

Procedural guidelines for disclosure of incidental genomic information are lacking. We introduce a method and evaluated the impact of returning results to population biobank participants with 16p11.2 copy number variants, which are commonly associated with neurodevelopmental disorders and BMI imbala...

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Bibliographic Details

Published in:	Personalized medicine Vol. 13; no. 4; p. 303
Main Authors:	Leitsalu, Liis, Alavere, Helene, Jacquemont, Sébastien, Kolk, Anneli, Maillard, Anne M, Reigo, Anu, Nõukas, Margit, Reymond, Alexandre, Männik, Katrin, Ng, Pauline C, Metspalu, Andres
Format:	Journal Article
Language:	English
Published:	England 01.07.2016
Subjects:	return of results incidental findings 16p11.2 CNV genomic disorders population biobank
ISSN:	1741-0541, 1744-828X, 1744-828X
Online Access:	Get more information
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