Abstract
Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.
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https://doi.org/10.1002/(sici)1098-1004(1997)10:1<80::aid-humu12>3.0.co;2-w
Copy DOIJournal: Human Mutation | Publication Date: Jan 1, 1997 |
Citations: 2 |
Identification of a one-base germline deletion (codon 888 del C) and an intron splice acceptor site polymorphism in hMSH2.
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