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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Detalles Bibliográficos
Autores principales: Willie, Delayna, Holmes, Greg, Jabs, Ethylin Wang, Wu, Meng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9397066/
https://www.ncbi.nlm.nih.gov/pubmed/35997397
http://dx.doi.org/10.3390/jdb10030033

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9397066/
https://www.ncbi.nlm.nih.gov/pubmed/35997397
http://dx.doi.org/10.3390/jdb10030033

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