RNA Analysis Identifies Pathogenic Duplications in MSH2 in Patients With Lynch Syndrome
Author:
Publisher
Elsevier BV
Subject
Gastroenterology,Hepatology
Reference11 articles.
1. NCCN. NCCN clinical practice guidelines in oncology V.3.2017: Genetic/Familial High-Risk Assessment: Colorectal. NCCN Clinical Practice Guidelines 2017.
2. Characterization of novel, large duplications in the MSH2 gene of three unrelated Lynch syndrome patients
3. Pathological Consequences of Sequence Duplications in the Human Genome
4. DNA breakpoint assay reveals a majority of gross duplications occur in tandem reducing VUS classifications in breast cancer predisposition genes
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