| Literature DB >> 9818897 |
P M Bingham1, D Lynch, D McDonald-McGinn, E Zackai.
Abstract
We report two children with chromosome 22q11 deletion syndrome who had neuroradiologic evidence of polymicrogyria. The diagnosis of chromosome 22q11 deletion should be considered in individuals with polymicrogyria.Entities:
Mesh:
Year: 1998 PMID: 9818897 DOI: 10.1212/wnl.51.5.1500
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910