Neurofibromatosis in a man with a ring 22: In situ hybridization studies
- 1 March 1987
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 25 (1) , 169-174
- https://doi.org/10.1016/0165-4608(87)90173-7
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Malignancy in NeurofibromatosisPublished by S. Karger AG ,2015
- A genetic linkage study in 15 families of individuals with von Recklinghausen neurofibromatosisAmerican Journal of Medical Genetics, 1985
- A familial pericentric inversion of chromosome 22 with a recombinant subject illustrating a 'pure' partial monosomy syndrome.Journal of Medical Genetics, 1985
- Localization of the cellular oncogenes ABL, SIS, and FES on human germ-line chromosomesCytogenetic and Genome Research, 1984
- Linkage analysis of neurofibromatosis (von Recklinghausen disease).Journal of Medical Genetics, 1983
- Neurofibromatosis: Clinical heterogeneityCurrent Problems in Cancer, 1982
- A human onc gene homologous to the transforming gene (v-sis) of simian sarcoma virusNature, 1981
- Localization of single copy DNA sequences on G-banded human chromosomes by in situ hybridizationChromosoma, 1981
- Phenotypic correlations in patients with ring chromosome 22Clinical Genetics, 1977