Wu, Xiao-Lin <br/><br/>
Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.  [electronic resource] 

 -  American journal of human genetics  Jul 2009 
 - 53-63 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2009.06.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Aged<br/>Amino Acid Sequence<br/>Animals<br/>Child<br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Exons<br/>Female<br/>Fibroblast Growth Factor 9--chemistry<br/>Humans<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Pedigree<br/>Signal Transduction<br/>Synostosis--genetics