Article
Progress toward the isolation and characterization of the genes causing neurofibromatosis.
Brain pathology (Zurich, Switzerland) - 1 Sept 1990
Menon A G, Gusella J F, Seizinger B R
Abstract excerpt
Neurofibromatosis 1 and neurofibromatosis 2 are clinically distinct autosomal dominant disorders that affect an estimated 1.5 million individuals throughout the world. The genetic defect in each disorder has been mapped to different chromosomes, NF1 to chromosome 17 and NF2 to chromosome 22. Prog...
Topics
- Chromosome Aberrations
- Chromosome Mapping
- Chromosomes, Human, Pair 17
- Chromosomes, Human, Pair 22
- Cloning, Molecular
- Gene Expression Regulation, Neoplastic
- Genes, Dominant
- Genes, Neurofibromatosis 1
- Genes, Neurofibromatosis 2
- Genetic Markers
- Humans
- Mutation
- Neurofibromatosis 1
- Neurofibromatosis 2
- Parents
- Prevalence
