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...

Celý popis

Podrobná bibliografia

Vydané v:	Personalized medicine Ročník 13; číslo 4; s. 303
Hlavní autori:	Leitsalu, Liis, Alavere, Helene, Jacquemont, Sébastien, Kolk, Anneli, Maillard, Anne M, Reigo, Anu, Nõukas, Margit, Reymond, Alexandre, Männik, Katrin, Ng, Pauline C, Metspalu, Andres
Médium:	Journal Article
Jazyk:	English
Vydavateľské údaje:	England 01.07.2016
Predmet:	return of results incidental findings 16p11.2 CNV genomic disorders population biobank
ISSN:	1741-0541, 1744-828X, 1744-828X
On-line prístup:	Zistit podrobnosti o prístupe
Tagy:	Pridať tag Žiadne tagy, Buďte prvý, kto otaguje tento záznam!