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From shape to cells: mouse models reveal mechanisms altering palate development in Apert syndrome
Apert syndrome is a congenital disorder characterized by severe skull malformations and caused by one of two missense mutations, S252W and P253R, on fibroblast growth factor receptor 2 (FGFR2). The molecular bases underlying differential Apert syndrome phenotypes are still poorly understood and it i...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Limited
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3634659/ https://ncbi.nlm.nih.gov/pubmed/23519026 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.010397 |
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