Mutations inMLH1 are more frequent than inMSH2 in sporadic colorectal cancers with microsatellite instability
- 1 January 1997
- journal article
- research article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 18 (1) , 42-49
- https://doi.org/10.1002/(sici)1098-2264(199701)18:1<42::aid-gcc5>3.0.co;2-1
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Genomic structure of human mismatch repair gene, hMLH1, and its mutation analysis in patients with hereditary non-polyposis colorectal cancer (HNPCC)Human Molecular Genetics, 1995
- Loss of the wild type MLH1 gene is a feature of hereditary nonpolyposis colorectal cancerNature Genetics, 1994
- Structure of the Human MSH2 Locus and Analysis of Two Muir-Torre Kindreds for msh2 MutationsGenomics, 1994
- Mutation in the DNA mismatch repair gene homologue hMLH 1 is associated with hereditary non-polyposis colon cancerNature, 1994
- Familial adenomatous polyposis (FAP): Frequency, penetrance, and mutation rateHuman Mutation, 1994
- The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancerCell, 1993
- Mutations in the RET proto-oncogene are associated with MEN 2A and FMTCHuman Molecular Genetics, 1993
- Ubiquitous somatic mutations in simple repeated sequences reveal a new mechanism for colonic carcinogenesisNature, 1993
- A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studiesNucleic Acids Research, 1991
- A Pseudoautosomal Gene in ManScience, 1986