Sanna-Cherchi, Simone <br/><br/>
Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.  [electronic resource] 

 -  American journal of human genetics  12 2017 
 - 1034 p.  digital 
<br/><br/> Publication Type: Journal Article; Published Erratum 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2017.11.003  doi