Patients with an unexplained microsatellite instable tumour have a low risk of familial cancer

This publication has 35 references indexed in Scilit:

• MLH1 germline epimutations in selected patients with early‐onset non‐polyposis colorectal cancer
  Clinical Genetics, 2007
• Identification of mismatch repair gene mutations in young patients with colorectal cancer and in patients with multiple tumours associated with hereditary non-polyposis colorectal cancer
  Gut, 2006
• Very low prevalence of germline MSH6 mutations in hereditary non-polyposis colorectal cancer suspected patients with colorectal cancer without microsatellite instability
  British Journal of Cancer, 2006
• CpG island methylator phenotype underlies sporadic microsatellite instability and is tightly associated with BRAF mutation in colorectal cancer
  Nature Genetics, 2006
• Spectrum and frequencies of mutations inMSH2 andMLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer
  International Journal of Cancer, 2005
• Screening for the Lynch Syndrome (Hereditary Nonpolyposis Colorectal Cancer)
  New England Journal of Medicine, 2005
• Molecular Analysis of Hereditary Nonpolyposis Colorectal Cancer in the United States: High Mutation Detection Rate among Clinically Selected Families and Characterization of an American Founder Genomic Deletion of the MSH2 Gene
  American Journal of Human Genetics, 2003
• Description and functional analysis of a novel in frame mutation linked to hereditary non-polyposis colorectal cancer
  Journal of Medical Genetics, 2002
• MSH2 andMLH1 mutations in sporadic replication error-positive colorectal carcinoma as assessed by two-dimensional DNA electrophoresis
  Genes, Chromosomes and Cancer, 1997
• The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
  Diseases of the Colon & Rectum, 1991