PubMed:15951966 / 0-196 JSONTXT

{"target":"https://pubannotation.org/docs/sourcedb/PubMed/sourceid/15951966","sourcedb":"PubMed","sourceid":"15951966","source_url":"http://www.ncbi.nlm.nih.gov/pubmed/15951966","text":"Screening for exonic copy number mutations at MSH2 and MLH1 by MAPH.\nBACKGROUND: Exonic deletions in MSH2 and MLH1 are significant contributors to the mutation spectrum in HNPCC, and heterozygous 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