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Objective: 3p deletion syndrome is a rare monosomal disease that encompasses deletions throughout the short arm of chromosome 3. It is often in the distal region (3p25-pter), but variations in ...

Dysmorphic facial features were reported in 42/54 and were consistent with those previously noted,22 with widely spaced eyes (hypertelorism, broad nasal bridge and/or telecanthus) and ear anomalies ...