D'Alessandro, Lisa C A <br/><br/>
Exome sequencing identifies rare variants in multiple genes in atrioventricular septal defect.  [electronic resource] 

 -  Genetics in medicine : official journal of the American College of Medical Genetics  Feb 2016 
 - 189-98 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1530-0366 
<br/><br/><label>Standard No.: </label>10.1038/gim.2015.60  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Exome<br/>Female<br/>Genetic Variation<br/>Genotype<br/>Heart Septal Defects--genetics<br/>Humans<br/>Male<br/>Mutation<br/>Phenotype<br/>Sequence Analysis, DNA