Value of MLH1 and MSH2 Mutations in the Appearance of Muir–Torre Syndrome Phenotype in HNPCC Patients Presenting Sebaceous Gland Tumors or Keratoacanthomas
- 1 October 2006
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 126 (10) , 2302-2307
- https://doi.org/10.1038/sj.jid.5700475
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Cancer Risk in Hereditary Nonpolyposis Colorectal Cancer Syndrome: Later Age of OnsetGastroenterology, 2005
- Identification of Muir–Torre syndrome among patients with sebaceous tumors and keratoacanthomasCancer, 2005
- A genotype-phenotype correlation in HNPCC: strong predominance of msh2 mutations in 41 patients with Muir-Torre syndromeJournal of Medical Genetics, 2004
- A founder MLH1 mutation in families from the districts of Modena and Reggio-Emilia in northern Italy with hereditary non-polyposis colorectal cancer associated with protein elongation and instabilityJournal of Medical Genetics, 2004
- Frequency of Microsatellite Instability in Unselected Sebaceous Gland Neoplasias and HyperplasiasJournal of Investigative Dermatology, 2003
- Four novelMSH2 andMLH1 frameshift mutations and occurrence of a breast cancer phenocopy in hereditary nonpolyposis colorectal cancerHuman Mutation, 2001
- Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosisGut, 1999
- Genitourinary tumors in men with the Muir-Torre syndromeJournal of the American Academy of Dermatology, 1995
- The Muir-Torre syndrome: A 25-year retrospectJournal of the American Academy of Dermatology, 1995
- The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)Diseases of the Colon & Rectum, 1991