SATB2-associated syndrome: a case report
Introduction: SATB2-associated syndrome is an extremely rare genetic disorder. It is characterized by delayed neurocognitive development, craniofacial anomalies and dental defects. Observation: This case report highlights the craniofacial and dental phenotype linked to a mutation resulting in SATB2-...
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| Main Authors: | , , , |
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| Format: | Book |
| Published: |
EDP Sciences,
2024-01-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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