Samocha, Kaitlin E <br/><br/>
A framework for the interpretation of de novo mutation in human disease.  [electronic resource] 

 -  Nature genetics  Sep 2014 
 - 944-50 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.3050  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child Development Disorders, Pervasive--genetics<br/>Exome<br/>Female<br/>Genetic Code<br/>Genetic Predisposition to Disease<br/>Genetics, Medical--methods<br/>Humans<br/>Male<br/>Mutation