Sensitive Detection of Deletions of One or More Exons in the Neurofibromatosis Type 2 (NF2) Gene by Multiplexed Gene Dosage Polymerase Chain Reaction
- 28 February 2005
- journal article
- research article
- Published by Elsevier in The Journal of Molecular Diagnostics
- Vol. 7 (1) , 97-104
- https://doi.org/10.1016/s1525-1578(10)60014-1
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Somatic mosaicism in neurofibromatosis 2: prevalence and risk of disease transmission to offspringJournal of Medical Genetics, 2003
- Molecular genetic analysis of the NF2 gene in young patients with unilateral vestibular schwannomasJournal of Medical Genetics, 2002
- High Frequency of Large Intragenic Deletions in the Fanconi Anemia Group A GeneAmerican Journal of Human Genetics, 1999
- Characterisation of 16 polymorphic markers in theNF2 gene: Application to hemizygosity detectionHuman Mutation, 1999
- Somatic Mosaicism: A Common Cause of Classic Disease in Tumor-Prone Syndromes? Lessons from Type 2 NeurofibromatosisAmerican Journal of Human Genetics, 1998
- Isolation and Characterization of Schwann Cells from Neurofibromatosis Type 2 PatientsNeurobiology of Disease, 1998
- Predominant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomasGenes, Chromosomes and Cancer, 1995
- Exon scanning for mutation of the NF2 gene in schwannomasHuman Molecular Genetics, 1994
- Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuromaNature, 1986
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971