Gastrointestinal cancers and neurofibromatosis type 1 features in children with a germline homozygous MLH1 mutation
- 1 February 2004
- journal article
- case report
- Published by Elsevier in Gastroenterology
- Vol. 126 (2) , 576-585
- https://doi.org/10.1053/j.gastro.2003.11.008
Abstract
No abstract availableKeywords
This publication has 29 references indexed in Scilit:
- Early-Onset Brain Tumor and Lymphoma in MSH2-Deficient ChildrenAmerican Journal of Human Genetics, 2003
- Impact of microsatellite testing and mismatch repair protein expression on the clinical interpretation of genetic testing in hereditary non-polyposis colorectal cancerZeitschrift für Krebsforschung und Klinische Onkologie, 2002
- Mutations of hMLH1 and hMSH2 in Patients With Suspected Hereditary Nonpolyposis Colorectal Cancer: Correlation With Microsatellite Instability and Abnormalities of Mismatch Repair Protein ExpressionJournal of Clinical Oncology, 2002
- Loss of DNA Mismatch Repair Proteins in Skin Tumors From Patients With Muir–Torre Syndrome and MSH2 or MLH1 Germline MutationsThe American Journal of Surgical Pathology, 2002
- The Frequency of Hereditary Defective Mismatch Repair in a Prospective Series of Unselected Colorectal CarcinomasAmerican Journal of Human Genetics, 2001
- Genotype-Phenotype Correlations in Attenuated Adenomatous Polyposis ColiAmerican Journal of Human Genetics, 1998
- The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2Published by American Medical Association (AMA) ,1997
- Structure of the Human MSH2 Locus and Analysis of Two Muir-Torre Kindreds for msh2 MutationsGenomics, 1994
- The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)Diseases of the Colon & Rectum, 1991
- Villous tumors of the duodenum and jejunumDigestive Diseases and Sciences, 1973