Meckel’s Cartilage in Mandibular Development and Dysmorphogenesis

The Fgfr2c ( C342Y/+ ) Crouzon syndrome mouse model carries a cysteine to tyrosine substitution at amino acid position 342 (Cys342Tyr; C342Y) in the fibroblast growth factor receptor 2 (Fgfr2) gene equivalent to a FGFR2 mutation commonly associated with Crouzon and Pfeiffer syndromes in humans. The...

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Detalles Bibliográficos
Autores principales: Pitirri, M. Kathleen, Durham, Emily L., Romano, Natalie A., Santos, Jacob I., Coupe, Abigail P., Zheng, Hao, Chen, Danny Z., Kawasaki, Kazuhiko, Jabs, Ethylin Wang, Richtsmeier, Joan T., Wu, Meng, Motch Perrine, Susan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9149363/
https://www.ncbi.nlm.nih.gov/pubmed/35651944
http://dx.doi.org/10.3389/fgene.2022.871927

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9149363/
https://www.ncbi.nlm.nih.gov/pubmed/35651944
http://dx.doi.org/10.3389/fgene.2022.871927

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