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
- 19 May 1997
- journal article
- case report
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 234 (2) , 346-350
- https://doi.org/10.1006/bbrc.1997.6645
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Identification of NF1 mutations in both alleles of a dermal neurofibromaNature Genetics, 1996
- Clonality of tuberous sclerosis harmatomas shown by non-random X-chromosome inactivationHuman Genetics, 1996
- Loss of NF1 results in activation of the Ras signaling pathway and leads to aberrant growth in haematopoietic cellsNature Genetics, 1996
- Benign neurofibromas in type 1 neurofibromatosis (NF1) show somatic deletions of the NF1 geneNature Genetics, 1995
- 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
- Two CA/GT repeat polymorphisms in intron 27 of the human neurofibromatosis type 1 (NF1) geneHuman Genetics, 1994
- 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
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971
- Multiple Cell Origin of Hereditary NeurofibromasNew England Journal of Medicine, 1971