Interstitial deletion of 11 (P11.2p12): A newly described contiguous gene deletion syndrome involving the gene for hereditary multiple exostoses (EXT2)
- 29 March 1996
- journal article
- review article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 62 (3) , 319-325
- https://doi.org/10.1002/(sici)1096-8628(19960329)62:3<319::aid-ajmg22>3.0.co;2-m
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2)Journal of Medical Genetics, 1995
- Cloning of the putative tumour suppressor gene for hereditary multiple exostoses (EXT1)Nature Genetics, 1995
- The 1993–94 Généthon human genetic linkage mapNature Genetics, 1994
- A gene for hereditary multiple exostoses maps to chromosome 19pHuman Molecular Genetics, 1994
- Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7Human Molecular Genetics, 1993
- Hereditary multiple exostoses.Journal of Medical Genetics, 1991
- An unusual type of acrocephalosyndactyly with bilateral parietooccipital “encephalocele”, micropenis, and severe mental retardationAmerican Journal of Medical Genetics, 1990
- Microdeletion syndromes, balanced translocations, and gene mapping.Journal of Medical Genetics, 1988
- Chromosome deletion and multiple cartilaginous exostosesEuropean Journal of Pediatrics, 1980
- Gene dose effect: intraband mapping of the LDH A locus using cells from four individuals with different interstitial deletions of 11pCytogenetic and Genome Research, 1977