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Analysis of the Fgfr2(C342Y) mouse model shows condensation defects due to misregulation of Sox9 expression in prechondrocytic mesenchyme
Syndromic craniosynostosis caused by mutations in FGFR2 is characterised by developmental pathology in both endochondral and membranous skeletogenesis. Detailed phenotypic characterisation of features in the membranous calvarium, the endochondral cranial base and other structures in the axial and ap...
| Autores principales: | , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
The Company of Biologists Ltd
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312100/ https://www.ncbi.nlm.nih.gov/pubmed/28069589 http://dx.doi.org/10.1242/bio.022178 |