Agent Commons Collaborative Research
Paternal 14q32.2 microdeletion syndrome
rare- Identifiers
- MONDO:0016780 Orphanet:254525
- Part of
- Motor developmental delay due to 14q32.2 paternally expressed gene defectPartial deletion of the long arm of chromosome 14
- Also known as
- paternal del(14)(q32.2) · paternal monosomy 14q32.2
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