Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer
- 1 January 2000
- journal article
- Published by Elsevier in European Journal Of Cancer
- Vol. 36 (1) , 49-54
- https://doi.org/10.1016/s0959-8049(99)00208-7
Abstract
No abstract availableKeywords
This publication has 22 references indexed in Scilit:
- HNPCC associated with germline mutation in the TGF-β type II receptor geneNature Genetics, 1998
- Microsatellite instability and mutation analysis of hMSH2 and hMLH1 in patients with sporadic, familial and hereditary colorectal cancerHuman Molecular Genetics, 1996
- Molecular Mechanisms Underlying Hereditary Nonpolyposis Colorectal CarcinomaJNCI Journal of the National Cancer Institute, 1996
- Analysis of mismatch repair genes in hereditary non–polyposis colorectal cancer patientsNature Medicine, 1996
- Hereditary Nonpolyposis Colorectal Cancer: the Syndrome, the Genes, and Historical PerspectivesJNCI Journal of the National Cancer Institute, 1995
- Role of clinical criteria in the diagnosis of hereditary non‐polyposis colorectal cancer (HNPCC): Results of a multivariate analysisInternational Journal of Cancer, 1994
- Mutations of two P/WS homologues in hereditary nonpolyposis colon cancerNature, 1994
- Mutation of a mutL Homolog in Hereditary Colon CancerScience, 1994
- Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancerPublished by Elsevier ,1993
- Frequency of hereditary colorectal carcinomaGastroenterology, 1987