Oldridge, M <br/><br/>
Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome.  [electronic resource] 

 -  Human molecular genetics  Jun 1995 
 - 1077-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/4.6.1077  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Base Sequence<br/>Craniofacial Dysostosis--genetics<br/>DNA<br/>DNA Mutational Analysis<br/>Exons<br/>Female<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Receptor Protein-Tyrosine Kinases--genetics<br/>Receptor, Fibroblast Growth Factor, Type 2<br/>Receptors, Fibroblast Growth Factor--genetics<br/>Sequence Homology, Amino Acid