Physician interpretation of variants of uncertain significance
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cancer Research,Genetics (clinical),Oncology,Genetics
Link
http://link.springer.com/article/10.1007/s10689-018-0086-2/fulltext.html
Reference31 articles.
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4. Shields AE, Burke W, Levy DE (2008) Differential use of available genetic tests among primary care physicians in the U.S.: results of a national survey. Genet Med 10:404–414
5. Richards S, Aziz N, Bale S et al (2015) Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. Genet Med 17:405–424
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