Alberti, A <br/><br/>
1.5 Mb de novo 22q11.21 microduplication in a patient with cognitive deficits and dysmorphic facial features.  [electronic resource] 

 -  Clinical genetics  Feb 2007 
 - 177-82 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2007.00750.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aneuploidy<br/>Child, Preschool<br/>Chromosomes, Human, Pair 22--genetics<br/>Craniofacial Abnormalities--genetics<br/>DiGeorge Syndrome--genetics<br/>Female<br/>Humans<br/>Intellectual Disability--genetics<br/>Phenotype<br/>Syndrome<br/>Tandem Repeat Sequences