Malbin, Jamileh <br/><br/>
Cryptic de novo deletion at 2q23.3-q24.1 in a patient with intellectual disability.  [electronic resource] 

 -  Journal of genetics  Jun 2016 
 - 441-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0973-7731 
<br/><br/><label>Standard No.: </label>10.1007/s12041-016-0630-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 2<br/>Comparative Genomic Hybridization<br/>Female<br/>Humans<br/>Intellectual Disability--diagnosis<br/>Nucleic Acid Amplification Techniques<br/>Pedigree<br/>Seizures--diagnosis<br/>Self-Injurious Behavior--physiopathology<br/>Speech Intelligibility