Growth pattern in the Apert syndrome
Birth prevalence study of the Apert syndrome
Skeletal abnormalities in the Apert syndrome.
Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases
Apert Syndrome Mutations in Fibroblast Growth Factor Receptor 2 Exhibit increased Affinity for FGF Ligand
Exclusive paternal origin of new mutations in Apert syndrome
Analysis of phenotypic features and FGFR2 mutations in Apert syndrome.
Structural basis for fibroblast growth factor receptor 2 activation in Apert syndrome
The definitive plastic surgical treatment of the severe facial deformities of craniofacial dysostosis. Crouzon's and Apert's diseases.
