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Article

Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer

1 Nov 1997

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Share to Colorectal Cancer Screening and Detection
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9354786
DOI: 10.1038/ng1197-271

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Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancerPMID 9354786Read ↗

Cancer risk in hereditary nonpolyposis colorectal cancer due to MSH6 mutations: impact on counseling and surveillanceSemantic proximity Read ↗

Association of Hereditary Nonpolyposis Colorectal Cancer–Related Tumors Displaying Low Microsatellite Instability with MSH6 Germline MutationsSemantic proximity Read ↗

Novel germline and somatic mutations of the MSH2 gene in hereditary non-polyposis colorectal cancer.Semantic proximity Read ↗

Identification of a novel MSH6 germline variant in a family with multiple gastro-intestinal malignancies by next generation sequencing.Semantic proximity Read ↗

Cancer Risks Associated With Germline Mutations in MLH1, MSH2, and MSH6 Genes in Lynch SyndromeSemantic proximity Read ↗

Heritable germline epimutation of MSH2 in a family with hereditary nonpolyposis colorectal cancerSemantic proximity Read ↗

An unusual tumor spectrum in Lynch syndrome caused by MSH6 mutationSemantic proximity Read ↗

[Single nucleotide polymorphism analysis of germline MSH6 gene mutations in Chinese hereditary non-polyposis colorectal cancer probands].Semantic proximity Read ↗

Recently identified colon cancer predispositions: MYH and MSH6 mutations.Semantic proximity Read ↗

Three novel missense germline mutations in different exons of MSH6 gene in Chinese hereditary non-polyposis colorectal cancer families.Semantic proximity Read ↗

A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitisSemantic proximity Read ↗

Familial endometrial cancer in female carriers of MSH6 germline mutationsSemantic proximity Read ↗

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