Nizon, Mathilde <br/><br/>
IMPAD1 mutations in two Catel-Manzke like patients.  [electronic resource] 

 -  American journal of medical genetics. Part A  Sep 2012 
 - 2183-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.35504  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Hand Deformities, Congenital--enzymology<br/>Humans<br/>Mutation<br/>Phosphoric Monoester Hydrolases--genetics<br/>Pierre Robin Syndrome--enzymology