Wohlleber, Eva <br/><br/>
Clinical and molecular characterization of two patients with overlapping de novo microdeletions in 2p14-p15 and mild mental retardation.  [electronic resource] 

 -  European journal of medical genetics   
 - 67-72 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2010.09.012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 12--genetics<br/>Comparative Genomic Hybridization<br/>Databases, Genetic<br/>Female<br/>Gene Dosage<br/>Humans<br/>Intellectual Disability--pathology<br/>Karyotyping<br/>Male