Mei, Davide <br/><br/>
Xp22.3 genomic deletions involving the CDKL5 gene in girls with early onset epileptic encephalopathy.  [electronic resource] 

 -  Epilepsia  Apr 2010 
 - 647-54 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1528-1167 
<br/><br/><label>Standard No.: </label>10.1111/j.1528-1167.2009.02308.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Alleles<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>DNA Mutational Analysis<br/>Developmental Disabilities--diagnosis<br/>Epilepsy--diagnosis<br/>Female<br/>Gene Duplication<br/>Genetic Testing<br/>Humans<br/>Infant<br/>Rett Syndrome--diagnosis<br/>Spasms, Infantile--diagnosis<br/>Young Adult