Purushothaman, Roopa <br/><br/>
Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes.  [electronic resource] 

 -  Birth defects research. Part A, Clinical and molecular teratology  Jul 2011 
 - 603-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1542-0760 
<br/><br/><label>Standard No.: </label>10.1002/bdra.20811  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acrocephalosyndactylia--genetics<br/>Animals<br/>Craniosynostoses--genetics<br/>Disease Models, Animal<br/>Face--pathology<br/>Female<br/>Male<br/>Maxilla--pathology<br/>Mice<br/>Osteogenesis<br/>Receptor, Fibroblast Growth Factor, Type 1--genetics<br/>Receptor, Fibroblast Growth Factor, Type 2--genetics<br/>Skull Base--pathology