Inan, Cihan <br/><br/>
Schizencephaly accompanied by occipital encephalocele and deletion of chromosome 22q13.32: a case report.  [electronic resource] 

 -  Fetal and pediatric pathology  Dec 2019 
 - 496-502 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1551-3823 
<br/><br/><label>Standard No.: </label>10.1080/15513815.2019.1604921  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Agenesis of Corpus Callosum--genetics<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 22<br/>Comparative Genomic Hybridization--methods<br/>Encephalocele--diagnosis<br/>Female<br/>Humans<br/>Schizencephaly--diagnosis<br/>Young Adult