Li, Feng <br/><br/>
3q29 interstitial microdeletion syndrome: an inherited case associated with cardiac defect and normal cognition.  [electronic resource] 

 -  European journal of medical genetics   
 - 349-52 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2009.05.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aortic Stenosis, Subvalvular--genetics<br/>Cells, Cultured<br/>Chromosome Breakage<br/>Chromosome Deletion<br/>Chromosomes, Artificial, Bacterial<br/>Chromosomes, Human, Pair 3<br/>Cognition<br/>Comparative Genomic Hybridization<br/>Databases as Topic<br/>Ductus Arteriosus, Patent--genetics<br/>Fathers<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Infant<br/>Lymphocytes--cytology<br/>Male<br/>Syndrome