Rossi, Massimiliano <br/><br/>
The appearance of the feet in Pfeiffer syndrome caused by FGFR1 P252R mutation.  [electronic resource] 

 -  Clinical dysmorphology  Oct 2003 
 - 269-74 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0962-8827 
<br/><br/><label>Standard No.: </label>10.1097/00019605-200310000-00012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acrocephalosyndactylia--genetics<br/>Child, Preschool<br/>Female<br/>Foot Deformities, Congenital--genetics<br/>Humans<br/>Point Mutation<br/>Receptor Protein-Tyrosine Kinases--genetics<br/>Receptor, Fibroblast Growth Factor, Type 1<br/>Receptors, Fibroblast Growth Factor--genetics<br/>Siblings