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Article

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

Human mutation - 1 Jan 1997

Swensen J, Lewis C M, Cannon-Albright L A

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Share to Colorectal Neoplasms, Hereditary Nonpolyposis
Share to DNA Repair
Share to Electrophoresis, Polyacrylamide Gel
Share to Germ-Line Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 9222765
DOI: 10.1002/(SICI)1098-1004(1997)10:1<80::AID-HUMU12>3.0.CO;2-W

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

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Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.PMID 9222765Read ↗

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