Ross, M E <br/><br/>
Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.  [electronic resource] 

 -  Human molecular genetics  Apr 1997 
 - 555-62 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/6.4.555  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cerebral Cortex--abnormalities<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 2--genetics<br/>Dosage Compensation, Genetic<br/>Epilepsy--etiology<br/>Female<br/>Genetic Linkage<br/>Humans<br/>Hybrid Cells<br/>In Situ Hybridization, Fluorescence<br/>Karyotyping<br/>Male<br/>Pedigree<br/>Phenotype<br/>Restriction Mapping<br/>Sex Chromosome Aberrations--genetics<br/>Translocation, Genetic<br/>X Chromosome--genetics