FBXO28is a critical gene of the 1q41q42 microdeletion syndrome
- 21 April 2015
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 167 (6), 1418-1420
- https://doi.org/10.1002/ajmg.a.37033
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Refinement of the critical region of 1q41q42 microdeletion syndrome identifies FBXO28 as a candidate causative gene for intellectual disability and seizuresAmerican Journal of Medical Genetics Part A, 2013
- Infantile epilepsy associated with mosaic 2q24 duplication including SCN2A and SCN3ASeizure, 2011
- New cases and refinement of the critical region in the 1q41q42 microdeletion syndromeEuropean Journal of Medical Genetics, 2011
- The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndromeGenetics in Medicine, 2007