Cartwright, Ashley <br/><br/>
Short case report: Xq23 deletion involving PAK3 as a novel cause of developmental delay in a 6-year-old boy.  [electronic resource] 

 -  Clinical dysmorphology  Jan 2017 
 - 38-40 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.0000000000000154  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, X<br/>Comparative Genomic Hybridization<br/>Developmental Disabilities--diagnosis<br/>Facies<br/>Genetic Association Studies<br/>Humans<br/>Male<br/>Phenotype<br/>p21-Activated Kinases--genetics