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Microsatellite instability and DNA mismatch repair protein deficiency in Lynch syndrome colorectal polyps.
Impact of genetic testing on endometrial cancer risk-reducing practices in women at risk for Lynch syndrome.
DNA Mismatch Repair
Germline TP53 Mutations in Patients With Early-Onset Colorectal Cancer in the Colon Cancer Family Registry.
Universal Screening for Mismatch-Repair Deficiency in Endometrial Cancers to Identify Patients With Lynch Syndrome and Lynch-like Syndrome.
Detection of Mismatch Repair Deficiency and Microsatellite Instability in Colorectal Adenocarcinoma by Targeted Next-Generation Sequencing.
Cancer Susceptibility Gene Mutations in Individuals With Colorectal Cancer.
Development and Validation of the PREMM5 Model for Comprehensive Risk Assessment of Lynch Syndrome.
Validation of a targeted next-generation sequencing approach to detect mismatch repair deficiency in colorectal adenocarcinoma.
Recent advances in Lynch syndrome.
Targeted Cancer Next-Generation Sequencing as a Primary Screening Tool for Microsatellite Instability and Lynch Syndrome in Upper Gastrointestinal Tract Cancers.
Clinical Factors Associated with Urinary Tract Cancer in Individuals with Lynch Syndrome.
Identification of Lynch syndrome by microsatellite instability and mismatch repair deficiency testing on colorectal adenomas.
Collaborative Group of the Americas on Inherited Gastrointestinal Cancer Position statement on multigene panel testing for patients with colorectal cancer and/or polyposis.
Comparison of Colorectal and Endometrial Microsatellite Instability Tumor Analysis and Premm5 Risk Assessment for Predicting Pathogenic Germline Variants on Multigene Panel Testing.
Familial Burden and Other Clinical Factors Associated With Various Types of Cancer in Individuals With Lynch Syndrome.
DNA Mismatch Repair