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Deletion of chromosome 22q11 is associated with the majority of cases of DiGeorge anomaly, velocardiofacial syndrome, and conotruncal anomaly face syndrome. This group of syndromes shares similar phenotypic characteristics related to abnormal neural crest development, including dysmorphic facial features, palatal abnormalities, thymic deficiency, hypocalcemia and conotruncal cardiac anomalies. The...
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