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Expression profiles of craniosynostosis-derived fibroblasts.

BACKGROUND: Craniosynostosis syndromes, a group of connective disorders characterized by abnormalities in vault osteogenesis and premature fusion of bone sutures, are associated with point mutations in FGF receptor family members. The cellular phenotype is characterized by abnormal extracellular mat...

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Detalhes bibliográficos
Main Authors: Carinci, Francesco, Bodo, Maria, Tosi, Lara, Francioso, Francesca, Evangelisti, Rita, Pezzetti, Furio, Scapoli, Luca, Martinelli, Marcella, Baroni, Tiziano, Stabellini, Giordano, Carinci, Paolo, Bellucci, Catia, Lilli, Cinzia, Volinia, Stefano
Formato: Artigo
Idioma:Inglês
Publicado em: 2002
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2039940/
https://ncbi.nlm.nih.gov/pubmed/12477974
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