Common skeletal features in rare diseases: New links between ciliopathies and FGF-related syndromes

Congenital skeletal anomalies are rare disorders, with a subset affecting both the cranial and appendicular skeleton. Two categories, craniosynostosis syndromes and chondrodysplasias, frequently result from aberrant regulation of the fibroblast growth factor (FGF) signaling pathway. Our recent work...

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Detalles Bibliográficos
Autores principales: Yannakoudakis, Basil Z, Liu, Karen J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Landes Bioscience 2013
Materias:
Addendum
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932950/
https://www.ncbi.nlm.nih.gov/pubmed/25003013
http://dx.doi.org/10.4161/rdis.27109

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932950/
https://www.ncbi.nlm.nih.gov/pubmed/25003013
http://dx.doi.org/10.4161/rdis.27109

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