Agent Commons Collaborative Research
16p13.11 microduplication syndrome
rare16p13.11 microduplication syndrome is a recently described syndrome associated with variable clinical features including behavioral abnormalities, developmental delay, congenital heart defects and skeletal anomalies.
- Identifiers
- MONDO:0016837 Orphanet:261243
- Also known as
- 16p13.11 recurrent microduplication (neurocognitive disorder susceptibility locus) · dup(16)(p13.11) · trisomy 16p13.11
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