Elevated Risk for MPNST in NF1 Microdeletion Patients
Top Cited Papers
Open Access
- 1 May 2003
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (5), 1288-1292
- https://doi.org/10.1086/374821
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Malignant peripheral nerve sheath tumours in neurofibromatosis 1Journal of Medical Genetics, 2002
- Malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1: a clinicopathologic and molecular study of 17 patients.2001
- Recombination hotspot in NF1 microdeletion patientsHuman Molecular Genetics, 2001
- Molecular studies in 20 submicroscopic neurofibromatosis type 1 gene deletionsHuman Mutation, 1999
- Constitutional and mosaic large NF1 gene deletions in neurofibromatosis type 1.Journal of Medical Genetics, 1998
- Deletion of the entireNF1 gene causing distinct manifestations in a familyAmerican Journal of Medical Genetics, 1997
- Deletions spanning the neurofibromatosis type 1 gene: Implications for genotype-phenotype correlations in neurofibromatosis type 1?Human Mutation, 1997
- Deletion of the entire NF1 gene detected by FISH: Four deletion patients associated with severe manifestationsAmerican Journal of Medical Genetics, 1995
- Malignant schwannoma of the head and neckThe American Journal of Surgery, 1992
- A genetic study of von Recklinghausen neurofibromatosis in south east Wales. I. Prevalence, fitness, mutation rate, and effect of parental transmission on severity.Journal of Medical Genetics, 1989