MSH2 c.1452–1455delAATG Is a Founder Mutation and an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Southern Chinese Population

This publication has 21 references indexed in Scilit:

• 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
• The Founder Mutation MSH2*1906G→C Is an Important Cause of Hereditary Nonpolyposis Colorectal Cancer in the Ashkenazi Jewish Population
  American Journal of Human Genetics, 2002
• Germline, somatic and epigenetic events underlying mismatch repair deficiency in colorectal and HNPCC-related cancers
  Oncogene, 2002
• A novel germline 1.8-kb deletion of hMLH1 mimicking alternative splicing: a founder mutation in the Chinese population
  Oncogene, 2001
• A New Statistical Method for Haplotype Reconstruction from Population Data
  American Journal of Human Genetics, 2001
• Recurrent germline mutation in MSH2 arises frequently de novo
  Journal of Medical Genetics, 2000
• Microsatellite Instability and Mutation of DNA Mismatch Repair Genes in Gliomas
  The American Journal of Pathology, 1998
• Incidence of Hereditary Nonpolyposis Colorectal Cancer and the Feasibility of Molecular Screening for the Disease
  New England Journal of Medicine, 1998
• Complex genetic predisposition to cancer in an extended HNPCC family with an ancestral hMLH1 mutation.
  Journal of Medical Genetics, 1996
• Genetic analysis of idiopathic torsion dystonia in Ashkenazi Jews and their recent descent from a small founder population
  Nature Genetics, 1995