Tumor LOH analysis provides reliable linkage information for prenatal genetic testing of sporadic NF1 patients
Author:
Publisher
Wiley
Subject
Cancer Research,Genetics
Reference26 articles.
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2. Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1;Ars;Hum Mol Genet,2000
3. Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 gene;Colman;Nat Genet,1995
4. Clonal origin of tumor cells in a plexiform neurofibroma with LOH in NF1 intron 38 and in dermal neurofibromas without LOH of the NF1 gene;Daschner;Biochem Biophys Res Commun,1997
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1. Dissecting loss of heterozygosity (LOH) in neurofibromatosis type 1-associated neurofibromas: Importance of copy neutral LOH;Human Mutation;2010-12-22
2. Analysis of NF1 somatic mutations in cutaneous neurofibromas from patients with high tumor burden;neurogenetics;2010-04-01
3. Mechanisms of Loss of Heterozygosity in Neurofibromatosis Type 1-Associated Plexiform Neurofibromas;Journal of Investigative Dermatology;2009-03
4. Mosaicism in sporadic neurofibromatosis type 1: variations on a theme common to other hereditary cancer syndromes?;Journal of Medical Genetics;2008-06-25
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