Abdalla, Ebtesam M <br/><br/>
A novel WNT10A mutation causes non-syndromic hypodontia in an Egyptian family.  [electronic resource] 

 -  Archives of oral biology  Jul 2014 
 - 722-8 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1879-1506 
<br/><br/><label>Standard No.: </label>10.1016/j.archoralbio.2014.04.004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Anodontia--genetics<br/>Cephalometry<br/>Child<br/>Egypt<br/>Female<br/>Heterozygote<br/>Humans<br/>MSX1 Transcription Factor--genetics<br/>Male<br/>Middle Aged<br/>Mutation<br/>PAX9 Transcription Factor--genetics<br/>Pedigree<br/>Polymorphism, Restriction Fragment Length<br/>Wnt Proteins--genetics