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pubmed-article:15118395pubmed:abstractTextHereditary nonpolyposis colorectal cancer (HNPCC) is an autosomal dominant disorder predisposing to predominantly colorectal cancer (CRC) and endometrial cancer frequently due to germline mutations in DNA mismatch repair (MMR) genes, mainly MLH1, MSH2 and also MSH6 in families seen to demonstrate an excess of endometrial cancer. As a consequence, tumors in HNPCC reveal alterations in the length of simple repetitive genomic sequences like poly-A, poly-T, CA or GT repeats (microsatellites) in at least 90% of the cases.lld:pubmed
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pubmed-article:15118395pubmed:copyrightInfoCopyright 2004 S. Karger AG, Basellld:pubmed
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pubmed-article:15118395pubmed:articleTitleExtended microsatellite analysis in microsatellite stable, MSH2 and MLH1 mutation-negative HNPCC patients: genetic reclassification and correlation with clinical features.lld:pubmed
pubmed-article:15118395pubmed:affiliationMedizinische Klinik und Poliklinik, Ludwig-Maximilians-Universität München, Munich, Germany. Uwe.Schiemann@med.uni-muenchen.delld:pubmed
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