Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome*
- 16 April 2002
- journal article
- research article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 109 (3) , 234-237
- https://doi.org/10.1002/ajmg.10314
Abstract
No abstract availableKeywords
Funding Information
- Deutsche Forschungsgemeinschaft (GRK336)
This publication has 4 references indexed in Scilit:
- Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epitheliumCytogenetic and Genome Research, 2000
- Costello syndrome with acoustic neuroma and cataract. Is the Costello locus linked to neurofibromatosis type 2 on 22q?Clinical Dysmorphology, 1998
- Hungarian case with Costello syndrome and translocation t(1,22)American Journal of Medical Genetics, 1995
- Genetics of the Costello syndromeAmerican Journal of Medical Genetics, 1994