You are here

14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.

Pubmed ID: 
22968132
Year: 
2013
Month: 
May
Volume: 
21
Issue: 
5
Citation: 
Ellaway CJ, Ho G, Bettella E, Knapman A, Collins F, Hackett A, McKenzie F, Darmanian A, Peters GB, Fagan K, Christodoulou J. 14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype. European journal of human genetics : EJHG 21 (5) : 522 - 7(2013) PubMed