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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 SyndromeAnálisis molecular de los exones 8, 9 y 10 del gen del factor de crecimiento de fibroblastos (FGFR2) en dos familias con casos índice de síndrome de Apert
(Universidad del Valle, 2015-09-30)
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 ...
