Subjects enrolled include over 4500 individuals; >3800 are patients with >300 different genetic syndromes with manifestations of craniofacial dysmorphology, as well as >600 apparently unaffected relatives. Enrolled subjects include males and females, with diverse age, racial, and ethnic composition. Available data include 3D morphometric facial scans (.ply format) and associated clinical and molecular genetic metadata. This is **restricted-access** human data. To gain access to these data, you must first go through the [process outlined here](/odocs/data-guidelines/).
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