Shinawi, M <br/><br/>
Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.  [electronic resource] 

 -  Clinical genetics  May 2015 
 - 478-82 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.12407  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Brain--pathology<br/>Calcium-Binding Proteins--genetics<br/>Child<br/>Chromosome Mapping<br/>Facies<br/>Female<br/>Genetic Association Studies<br/>Genetic Loci<br/>Genome-Wide Association Study<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Neurodevelopmental Disorders--diagnosis<br/>Phenotype<br/>Sequence Deletion<br/>Trans-Activators--genetics