Pilz, D T <br/><br/>
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.  [electronic resource] 

 -  Human molecular genetics  Dec 1998 
 - 2029-37 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/7.13.2029  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>1-Alkyl-2-acetylglycerophosphocholine Esterase<br/>Amino Acid Sequence<br/>Brain--abnormalities<br/>DNA--chemistry<br/>DNA Mutational Analysis<br/>Doublecortin Domain Proteins<br/>Doublecortin Protein<br/>Exons<br/>Female<br/>Genotype<br/>Humans<br/>Intellectual Disability--genetics<br/>Introns<br/>Male<br/>Microtubule-Associated Proteins<br/>Molecular Sequence Data<br/>Mutation<br/>Nervous System Malformations--genetics<br/>Neuropeptides--genetics<br/>Phenotype<br/>Proteins--genetics