Orbital Dysmorphology in Untreated Children with Crouzon and Apert Syndromes
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Ovid Technologies (Wolters Kluwer Health)
Reference46 articles.
1. Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
2. Genomic Screening of Fibroblast Growth-Factor Receptor 2 Reveals a Wide Spectrum of Mutations in Patients with Syndromic Craniosynostosis
3. Apert and Crouzon Syndromes: Clinical Findings, Genes and Extracellular Matrix
4. Ocular Manifestations of Apert and Crouzon Syndromes
5. Ophthalmic Findings in Apert’s Syndrome after Craniofacial SurgeryTwenty-nine Years’ Experience
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