Cordell, Heather J <br/><br/>
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.  [electronic resource] 

 -  Nature genetics  Jul 2013 
 - 822-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1546-1718 
<br/><br/><label>Standard No.: </label>10.1038/ng.2637  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Animals<br/>Case-Control Studies<br/>Chromosomes, Human, Pair 4--genetics<br/>Cohort Studies<br/>Female<br/>Genetic Loci<br/>Genetic Predisposition to Disease<br/>Genome-Wide Association Study<br/>Genotype<br/>Heart Defects, Congenital--genetics<br/>Heart Diseases--congenital<br/>Heart Septal Defects, Atrial--genetics<br/>Humans<br/>Male<br/>Mice<br/>Phenotype