Martínez-Jacobo, L <br/><br/>
Delineation of a de novo 7q21.3q31.1 Deletion by CGH-SNP Arrays in a Girl with Multiple Congenital Anomalies Including Severe Glaucoma.  [electronic resource] 

 -  Molecular syndromology  Sep 2013 
 - 285-91 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1661-8769 
<br/><br/><label>Standard No.: </label>10.1159/000353510  doi