Cleft Palate in Apert Syndrome
Apert syndrome is a rare genetic disorder characterized by craniosynostosis, midface retrusion, and limb anomalies. Cleft palate occurs in a subset of Apert syndrome patients. Although the genetic causes underlying Apert syndrome have been identified, the downstream signaling pathways and cellular m...
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| Principais autores: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
MDPI AG
2022-08-01
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| Series: | Journal of Developmental Biology |
| Assuntos: | |
| Acceso en liña: | https://www.mdpi.com/2221-3759/10/3/33 |
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