Wise, C A <br/><br/>
TCOF1 gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Apr 1997 
 - 3110-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.94.7.3110  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Cloning, Molecular<br/>DNA, Complementary<br/>Female<br/>Humans<br/>Male<br/>Mandibulofacial Dysostosis--genetics<br/>Molecular Sequence Data<br/>Mutation<br/>Nuclear Proteins--genetics<br/>Phosphoproteins--genetics<br/>Syndrome