Anthonappa, Robert P <br/><br/>
RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth.  [electronic resource] 

 -  Journal of investigative and clinical dentistry  May 2013 
 - 124-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>2041-1626 
<br/><br/><label>Standard No.: </label>10.1111/jicd.12019  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Cleidocranial Dysplasia--genetics<br/>Core Binding Factor Alpha 1 Subunit--genetics<br/>Female<br/>Humans<br/>Pedigree<br/>Tooth, Supernumerary--genetics