Quantification of Facial Skeletal Shape Variation in Fibroblast Growth Factor Receptor-Related Craniosynostosis Syndromes

BACKGROUND: fibroblast growth factor receptor (FGFR) -related craniosynostosis syndromes are caused by many different mutations within FGFR-1, 2, 3, and certain FGFR mutations are associated with more than one clinical syndrome. These syndromes share coronal craniosynostosis and characteristic facia...

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Detalhes bibliográficos
Main Authors: Heuzé, Yann, Martínez-Abadías, Neus, Stella, Jennifer M., Arnaud, Eric, Collet, Corinne, Fructuoso, Gemma García, Alamar, Mariana, Lo, Lun-Jou, Boyadjiev, Simeon A., Di Rocco, Federico, Richtsmeier, Joan T.
Formato: Artigo
Idioma:Inglês
Publicado em: 2014
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4029055/
https://ncbi.nlm.nih.gov/pubmed/24578066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/bdra.23228
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