Clinical implications of conflicting variant interpretations in the cancer genetics clinic
Author:
Funder
Myriad Genetics and Laboratories
National Institutes of Health
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference32 articles.
1. 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;Richards;Genet Med,2015
2. NCCN guidelines® insights: genetic/familial high-risk assessment: colorectal, version 1.2021;Weiss;J Natl Compr Canc Netw,2021
3. Association of risk-reducing surgery in BRCA1 or BRCA2 mutation carriers with cancer risk and mortality;Domchek;JAMA,2010
4. Recommendations for the care of individuals with an inherited predisposition to Lynch syndrome: a systematic review;Lindor;JAMA,2006
5. Essential elements of genetic cancer risk assessment, counseling, and testing: updated recommendations of the National Society of Genetic Counselors;Riley;J Genet Couns,2012
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