de Kovel, Carolien G F <br/><br/>
Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies.  [electronic resource] 

 -  Brain : a journal of neurology  Jan 2010 
 - 23-32 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Multicenter Study; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awp262  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 15--genetics<br/>Chromosomes, Human, Pair 16--genetics<br/>Cohort Studies<br/>Epilepsy, Generalized--etiology<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Humans<br/>Male<br/>Pedigree<br/>Young Adult