Saadi, Abdelkrim <br/><br/>
Compound heterozygous ASPM mutations associated with microcephaly and simplified cortical gyration in a consanguineous Algerian family.  [electronic resource] 

 -  European journal of medical genetics   
 - 180-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2009.03.013  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Algeria<br/>Birth Weight<br/>Cerebral Cortex--abnormalities<br/>Child<br/>Consanguinity<br/>Family<br/>Female<br/>Haplotypes<br/>Heterozygote<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Microcephaly--diagnostic imaging<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Pedigree<br/>Radiography<br/>Siblings