Unravelling the molecular control of calvarial suture fusion in children with craniosynostosis
<p>Abstract</p> <p>Background</p> <p>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 pathw...
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| Principais autores: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMC
2007-12-01
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| coleção: | BMC Genomics |
| Acesso em linha: | http://www.biomedcentral.com/1471-2164/8/458 |
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