Reardon, W <br/><br/>
Craniosynostosis associated with FGFR3 pro250arg mutation results in a range of clinical presentations including unisutural sporadic craniosynostosis.  [electronic resource] 

 -  Journal of medical genetics  Aug 1997 
 - 632-6 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-2593 
<br/><br/><label>Standard No.: </label>10.1136/jmg.34.8.632  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acrocephalosyndactylia--genetics<br/>Adult<br/>Arginine--genetics<br/>Child<br/>Child, Preschool<br/>Craniosynostoses--genetics<br/>Female<br/>Fibroblast Growth Factors--genetics<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Mutation<br/>Proline--genetics<br/>Protein-Tyrosine Kinases<br/>Receptor, Fibroblast Growth Factor, Type 3<br/>Receptors, Fibroblast Growth Factor--genetics