Al Turki, Saeed <br/><br/>
Rare variants in NR2F2 cause congenital heart defects in humans.  [electronic resource] 

 -  American journal of human genetics  04 2014 
 - 574-85 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.2014.03.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Binding Sites<br/>COUP Transcription Factor II--genetics<br/>Cell Line<br/>Exome<br/>Female<br/>Heart Defects, Congenital--genetics<br/>Humans<br/>Male<br/>Mice<br/>Mutation, Missense<br/>Pedigree<br/>Prospective Studies<br/>Transcription, Genetic