Reporting practices for variants of uncertain significance from next generation sequencing technologies-Reference-Cited by-同舟云学术

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Reporting practices for variants of uncertain significance from next generation sequencing technologies

Published:2017-10 Issue:10 Volume:60 Page:553-558
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Vears Danya F.,Sénécal Karine,Borry Pascal

Funder

Research Fund Flanders

Ministère de l’Économie, de la Science et de l’Innovation du Québec

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference18 articles.

1. The clinical application of genome-wide sequencing for monogenic diseases in Canada: position Statement of the Canadian College of Medical Geneticists;Boycott;J. Med. Genet.,2015

2. Recontacting in clinical practice: an investigation of the views of healthcare professionals and clinical scientists in the United Kingdom;Carrieri;Eur. J. Hum. Genet.,2017

3. Content analysis: method, applications, and issues;Downe-Wamboldt;Health Care Women Int.,1992

4. Qualitative content analysis in nursing research: concepts, procedures and measures to achieve trustworthiness;Graneheim;Nurse Educ. Today,2004

5. Mutation of TBCK causes a rare recessive developmental disorder;Guerreiro;Neurol. Genet.,2016

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