Akilapa, Rhoda S <br/><br/>
Clinical report: inherited deletion of chromosome 12q21.31q21.32 associated with a distinct phenotype and intellectual disability.  [electronic resource] 

 -  Clinical dysmorphology  Oct 2015 
 - 151-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1473-5717 
<br/><br/><label>Standard No.: </label>10.1097/MCD.0000000000000096  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 12<br/>DNA Copy Number Variations<br/>Genetic Association Studies<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Sequence Deletion