Vendrame, Martina <br/><br/>
Epilepsy in Prader-Willi syndrome: clinical characteristics and correlation to genotype.  [electronic resource] 

 -  Epilepsy & behavior : E&B  Nov 2010 
 - 306-10 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1525-5069 
<br/><br/><label>Standard No.: </label>10.1016/j.yebeh.2010.07.007  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>Electroencephalography<br/>Epilepsy--classification<br/>Female<br/>Genomic Imprinting<br/>Genotype<br/>Humans<br/>Infant<br/>Male<br/>Mutation<br/>Prader-Willi Syndrome--complications<br/>Retrospective Studies<br/>Risk Factors<br/>Statistics as Topic<br/>Young Adult