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Further Analysis of the Crouzon Mouse, Effects of the FGFR2(C342Y) Mutation are Cranial Bone Dependent
Crouzon syndrome is a debilitating congenital disorder involving abnormal craniofacial skeletal development caused by mutations in Fibroblast Growth Factor Receptor-2 (FGFR2). Phenotypic expression in humans exhibits an autosomal dominant pattern that commonly involves premature fusion of the corona...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3631296/ https://ncbi.nlm.nih.gov/pubmed/23358860 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00223-013-9701-2 |
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