Avila, M <br/><br/>
GLI3 is rarely implicated in OFD syndromes with midline abnormalities.  [electronic resource] 

 -  Human mutation  Nov 2011 
 - 1332-3 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't; Comment 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.21570  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Humans<br/>Kruppel-Like Transcription Factors--genetics<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Pallister-Hall Syndrome--pathology<br/>Polydactyly--pathology<br/>Syndactyly--pathology