Wang, Binbin <br/><br/>
Forkhead box H1 (FOXH1) sequence variants in ventricular septal defect.  [electronic resource] 

 -  International journal of cardiology  Nov 2010 
 - 83-5 p.  digital 
<br/><br/> Publication Type: Comparative Study; Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1874-1754 
<br/><br/><label>Standard No.: </label>10.1016/j.ijcard.2009.05.030  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Asian People--genetics<br/>Cohort Studies<br/>Forkhead Transcription Factors--genetics<br/>Genetic Variation--genetics<br/>Heart Septal Defects, Ventricular--diagnosis<br/>Humans<br/>Molecular Sequence Data<br/>Mutation--genetics