Orbital Dysmorphology in Untreated Children with Crouzon and Apert Syndromes
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Surgery
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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