"Molecular analysis of exons 8, 9 and 10 of the fibroblast growth factor receptor 2 (FGFR2) gene in two families with index cases of apert syndrome"

"Introduction: Apert syndrome (AS) is a craniosynostosis condition caused by mutations in the Fibroblast Growth Factor Receptor 2 (FGFR2) gene. Clinical features include cutaneous and osseous symmetric syndactily in hands and feet, with variable presentations in bones, brain, skin and other int...

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Detalles Bibliográficos
Autores Principales: Torres L., Hernández G., Barrera A., Ospina S., Prada R.
Formato: Artículo (Article)
Lenguaje:Inglés (English)
Publicado: Facultad de Salud de la Universidad del Valle 2015
Materias:
Acceso en línea:https://repository.urosario.edu.co/handle/10336/23734