Elias, Renata C <br/><br/>
Deletion of 17p13 and LIS1 gene mutation in isolated lissencephaly sequence.  [electronic resource] 

 -  Pediatric neurology  Jul 2006 
 - 42-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0887-8994 
<br/><br/><label>Standard No.: </label>10.1016/j.pediatrneurol.2005.12.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>1-Alkyl-2-acetylglycerophosphocholine Esterase<br/>Base Sequence<br/>Brain--abnormalities<br/>Child, Preschool<br/>Chromosomes, Human, Pair 17--genetics<br/>Female<br/>Gene Deletion<br/>Humans<br/>Infant<br/>Male<br/>Microtubule-Associated Proteins--genetics<br/>Polymorphism, Single-Stranded Conformational