Hempel, Maja <br/><br/>
Microdeletion syndrome 16p11.2-p12.2: clinical and molecular characterization.  [electronic resource] 

 -  American journal of medical genetics. Part A  Oct 2009 
 - 2106-12 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.33042  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 16<br/>Follow-Up Studies<br/>Humans<br/>Language Development Disorders--genetics<br/>Male<br/>Otitis--complications<br/>Syndrome