Browsing by Subject "22q11.2 deletion syndrome"
Now showing items 1-1 of 1
Variations in Craniofacial and Velopharyngeal Structures Among Individuals with 22q11.2 Deletion Syndrome (East Carolina University, 2016-07-25)22q11.2 deletion syndrome is the most common genetic cause of velopharyngeal dysfunction. Studies examining 22q11.2 deletion syndrome have thus far primarily focused on variations in the bony framework. Limited information ...