Toward a Survey of Somatic Mutation of the NF1 Gene in Benign Neurofibromas of Patients with Neurofibromatosis Type 1

This publication has 31 references indexed in Scilit:

• Loss ofNF1 allele in schwann cells but not in fibroblasts derived from an NF1-associated neurofibroma
  Genes, Chromosomes and Cancer, 1999
• Neurofibromatosis type 1 (NF1): a protein truncation assay yielding identification of mutations in 73% of patients.
  Journal of Medical Genetics, 1998
• Confirmation of a Double-Hit Model for the NF1Gene in Benign Neurofibromas
  American Journal of Human Genetics, 1997
• Identification of NF1 mutations in both alleles of a dermal neurofibroma
  Nature Genetics, 1996
• Site and sequence specific DNA methylation in the neurofibromatosis (NF1) gene includes C5839T: the site of the recurrent substitution mutation in exon 31
  Human Molecular Genetics, 1996
• Distribution of 13 truncating mutations in the neurofibromatosis 1 gene
  Human Molecular Genetics, 1995
• Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) gene
  Human Molecular Genetics, 1993
• Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesis
  Nature Genetics, 1993
• Methylation at dinucleotides other than CpG: implications for human maintenance methylation
  Gene, 1988
• Mutation and Cancer: Statistical Study of Retinoblastoma
  Proceedings of the National Academy of Sciences, 1971