Fofanova, O V <br/><br/>
A missense mutation of C1659 in the fibroblast growth factor receptor 3 gene in Russian patients with hypochondroplasia.  [electronic resource] 

 -  Endocrine journal  Dec 1998 
 - 791-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0918-8959 
<br/><br/><label>Standard No.: </label>10.1507/endocrj.45.791  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Child, Preschool<br/>Female<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation, Missense<br/>Osteochondrodysplasias--genetics<br/>Phenotype<br/>Protein-Tyrosine Kinases--chemistry<br/>Receptor, Fibroblast Growth Factor, Type 3<br/>Receptors, Fibroblast Growth Factor--chemistry<br/>Russia