Prevalence of germline mutations ofMLH1 andMSH2 in hereditary nonpolyposis colorectal cancer families from Spain

This publication has 32 references indexed in Scilit:

• Sensitivity and specificity of clinical criteria for hereditary non-polyposis colorectal cancer associated mutations in MSH2 and MLH1
  Journal of Medical Genetics, 2000
• Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer
  Nature Genetics, 1997
• Hereditary Nonpolyposis Colorectal Cancer Families Not Complying with the Amsterdam Criteria Show Extremely Low Frequency of Mismatch-Repair-Gene Mutations
  American Journal of Human Genetics, 1997
• DNA mismatch repair gene mutations in 55 kindreds with verified or putative hereditary non-polyposis colorectal cancer
  Human Molecular Genetics, 1996
• Hereditary Nonpolyposis Colorectal Cancer: the Syndrome, the Genes, and Historical Perspectives
  JNCI Journal of the National Cancer Institute, 1995
• Inactivation of the Type II TGF-β Receptor in Colon Cancer Cells with Microsatellite Instability
  Science, 1995
• Mutation of a mutL Homolog in Hereditary Colon Cancer
  Science, 1994
• Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancer
  Nature, 1994
• 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