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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Detaylı Bibliyografya
Asıl Yazarlar: Coussens, Anna K, Wilkinson, Christopher R, Hughes, Ian P, Morris, C Phillip, van Daal, Angela, Anderson, Peter J, Powell, Barry C
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: BioMed Central 2007
Konular:
Research Article
Online Erişim: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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