Mutations and Allelic Loss of the NF2 Gene in Neurofibromatosis 2-Associated Skin Tumors
- 1 May 2000
- journal article
- Published by Elsevier in Journal of Investigative Dermatology
- Vol. 114 (5) , 1017-1021
- https://doi.org/10.1046/j.1523-1747.2000.00975.x
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- What level of care for the neurofibromatoses?The Lancet, 1999
- Genotype/phenotype correlations in type 2 neurofibromatosis (NF2): evidence for more severe disease associated with truncating mutations.Journal of Medical Genetics, 1998
- Molecular Analysis of the NF2 Tumor-Suppressor Gene in SchwannomatosisAmerican Journal of Human Genetics, 1997
- The Diagnostic Evaluation and Multidisciplinary Management of Neurofibromatosis 1 and Neurofibromatosis 2JAMA, 1997
- Identification of NF2 germ-line mutations and comparison with neurofibromatosis 2 phenotypesHuman Genetics, 1996
- Frequency and distribution ofNF2 mutations in schwannomasGenes, Chromosomes and Cancer, 1996
- Highly polymorphic dinucleotide repeat at the NF2 geneHuman Genetics, 1995
- Analysis of mutations in the SCH gene in schwannomasGenes, Chromosomes and Cancer, 1994
- Exon scanning for mutation of the NF2 gene in schwannomasHuman Molecular Genetics, 1994
- A Clinical Study of Type 2 NeurofibromatosisQJM: An International Journal of Medicine, 1992