Gu, X-M <br/><br/>
PTCH mutations in sporadic and Gorlin-syndrome-related odontogenic keratocysts.  [electronic resource] 

 -  Journal of dental research  Sep 2006 
 - 859-63 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-0345 
<br/><br/><label>Standard No.: </label>10.1177/154405910608500916  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Asian People--genetics<br/>Basal Cell Nevus Syndrome--genetics<br/>China<br/>DNA Mutational Analysis<br/>Female<br/>Humans<br/>Keratins<br/>Male<br/>Middle Aged<br/>Mutation<br/>Odontogenic Cysts--genetics<br/>Patched Receptors<br/>Patched-1 Receptor<br/>Polymorphism, Genetic<br/>Receptors, Cell Surface--genetics