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Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development.

Human molecular genetics - 1 Nov 1994

Mary J L, Bishop T, Kolodner R, Lipford J R, Kane M, Weber W, Torhorst J, Müller H, Spycher M, Scott R J

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 7874129

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Mutational analysis of the hMSH2 gene reveals a three base pair deletion in a family predisposed to colorectal cancer development.PMID 7874129Read ↗

Gene symbol: hMSH2. Disease: Hereditary nonpolyposis colorectal cancer.Semantic proximity Read ↗

Genotype and phenotype of a new 2-bp deletion of hMSH2 at codon 233.Semantic proximity Read ↗

Intron splice acceptor site sequence variation in the hereditary non-polyposis colorectal cancer gene hMSH2.Semantic proximity Read ↗

A new mutation in the hMSH2 gene in a Spanish Lynch syndrome family.Semantic proximity Read ↗

Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.Semantic proximity Read ↗

Mutation of the hMSH2 gene in two families with hereditary nonpolyposis colorectal cancer.Semantic proximity Read ↗

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

Mismatch repair genes hMLH1 and hMSH2 and colorectal cancer: a HuGE review.Semantic proximity Read ↗

A novel missense germline mutation in exon 2 of the hMSH2 gene in a HNPCC family from Southern Italy.Semantic proximity Read ↗

Advances in the genetics and molecular biology of colorectal tumors.Semantic proximity Read ↗

The role of the human DNA mismatch repair gene hMSH2 in DNA repair, cell cycle control and apoptosis: implications for pathogenesis, progression and therapy of cancerSemantic proximity Read ↗

Pathogenicity of missense and splice site mutations in hMSH2 and hMLH1 mismatch repair genes: implications for genetic testing.Semantic proximity Read ↗

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