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Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeDOI 10.1016/j.yped.2011.10.021
Identification of new genetic alterations in MLH1, MSH2 and MSH6 using IHC and HRM analysis in Lynch syndrome-suspected patientsSemantic proximity
Cancer risks associated with germline mutations in MLH1, MSH2, and MSH6 genes in Lynch syndrome.Semantic proximity
Somatic Mutations in MLH1 and MSH2 Are a Frequent Cause of Mismatch-Repair Deficiency in Lynch Syndrome-Like TumorsSemantic proximity
An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutationSemantic proximity
Cancer risks in Lynch syndrome carriers: a systematic review and meta-analysis.Semantic proximity
Cancer risks for<i>MSH6</i>pathogenic variant carriersSemantic proximity
Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillanceSemantic proximity
Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome DatabaseSemantic proximity
Update on Lynch syndrome genomics.Semantic proximity
Early age of onset and broad cancer spectrum persist in MSH6- and PMS2-associated Lynch syndromeSemantic proximity
The changing landscape of Lynch syndrome due to PMS2 mutations.Semantic proximity
Risks of Lynch Syndrome Cancers for MSH6 Mutation CarriersSemantic proximity
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