Pathogenicity of the hereditary colorectal cancer mutation hMLH1 del616 linked to shortage of the functional protein

This publication has 26 references indexed in Scilit:

• Functional analysis ofMLH1mutations linked to hereditary nonpolyposis colon cancer
  Genes, Chromosomes and Cancer, 2001
• The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC) – Results of an international collaborative study
  Familial Cancer, 2001
• Genotype and phenotype in hereditary nonpolyposis colon cancer: a study of families with different vs. shared predisposing mutations
  Familial Cancer, 2001
• From the Cover: Loss of imprinting of the insulin-like growth factor II gene occurs by biallelic methylation in a core region of H19-associated CTCF-binding sites in colorectal cancer
  Proceedings of the National Academy of Sciences, 2000
• New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative Group on HNPCC
  Published by Elsevier ,1999
• MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis
  Genes, Chromosomes and Cancer, 1997
• DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer
  Human Molecular Genetics, 1996
• Genetic Mapping of a Locus Predisposing to Human Colorectal Cancer
  Science, 1993
• Clues to the Pathogenesis of Familial Colorectal Cancer
  Science, 1993
• The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
  Diseases of the Colon & Rectum, 1991