Heinzen, Erin L <br/><br/>
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.  [electronic resource] 

 -  American journal of human genetics  May 2010 
 - 707-18 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.2010.03.018  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosomes, Human, Pair 16<br/>Disease Susceptibility<br/>Epilepsy--genetics<br/>Humans<br/>Mutation<br/>Nucleic Acid Hybridization--genetics<br/>Sequence Deletion<br/>Syndrome