Towards a European consensus for reporting incidental findings during clinical NGS testing

In 2013, the American College of Medical Genetics (ACMG) examined the issue of incidental findings in whole exome and whole genome sequencing, and introduced recommendations to search for, evaluate and report medically actionable variants in a set of 56 genes. At a debate held during the 2014 Europe...

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Detaylı Bibliyografya
Yayımlandı:Eur J Hum Genet
Asıl Yazarlar: Hehir-Kwa, Jayne Y, Claustres, Mireille, Hastings, Ros J, van Ravenswaaij-Arts, Conny, Christenhusz, Gabrielle, Genuardi, Maurizio, Melegh, Béla, Cambon-Thomsen, Anne, Patsalis, Philippos, Vermeesch, Joris, Cornel, Martina C, Searle, Beverly, Palotie, Aarno, Capoluongo, Ettore, Peterlin, Borut, Estivill, Xavier, Robinson, Peter N
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2015
Konular:
Meeting Report
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4795187/
https://ncbi.nlm.nih.gov/pubmed/26036857
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.111
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