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Phenotype profile of a genetic mouse model for Muenke syndrome
PURPOSE: The Muenke syndrome mutation (FGFR3(P250R)), which was discovered 15 years ago, represents the single most common craniosynostosis mutation. Muenke syndrome is characterized by coronal suture synostosis, mid-face hypoplasia, subtle limb anomalies, and hearing loss. However, the spectrum of...
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| Autori principali: | , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2012
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4131982/ https://ncbi.nlm.nih.gov/pubmed/22872265 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00381-012-1778-9 |
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