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Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis
BACKGROUND: Craniosynostosis, the premature fusion of calvarial sutures, is a common craniofacial abnormality. Causative mutations in more than 10 genes have been identified, involving fibroblast growth factor, transforming growth factor beta, and Eph/ephrin signalling pathways. Mutations affect eac...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2007
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2222648/ https://ncbi.nlm.nih.gov/pubmed/18076769 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-8-458 |
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