Evidence for the Presence of the Second Allele of the Neurofibromatosis Type 1 Gene in Melanocytes Derived from Café au Lait Macules of NF1 Patients
- 8 August 1997
- journal article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 237 (1) , 138-141
- https://doi.org/10.1006/bbrc.1997.7097
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- Identification of NF1 mutations in both alleles of a dermal neurofibromaNature Genetics, 1996
- Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 geneNature Genetics, 1995
- An RsaI polymorphism in the transcribed region of the neurofibromatosis (NF1)-geneHuman Genetics, 1994
- Loss of The Normal NF1 Allele from the Bone Marrow of Children with Type 1 Neurofibromatosis and Malignant Myeloid DisordersNew England Journal of Medicine, 1994
- Novel alleles, hemizygosity and deletions at an Alu-repeat within the neurofibromatosis type 1 (NF1) geneHuman Molecular Genetics, 1993
- Somatic deletion of the neurofibromatosis type 1 gene in a neurofibrosarcoma supports a tumour suppressor gene hypothesisNature Genetics, 1993
- Loss of NF1 alleles in phaeochromocytomas from patients with type 1 neurofibromatosisGenes, Chromosomes and Cancer, 1992
- Increased melanogenesis in cultured epidermal melanocytes from patients with neurofibromatosis 1 (NF1)Human Genetics, 1991
- Human Melanocytes Cultured from Nevi and MelanomasJournal of Investigative Dermatology, 1986
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971