Crouzon syndrome: Genetic and intervention review
Author:
Publisher
Elsevier BV
Subject
General Dentistry,Otorhinolaryngology
Reference31 articles.
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3. Fibroblast growth factor (FGF) signaling in development and skeletal diseases;Teven;Genes Dis,2014
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5. Crouzon syndrome - a case report of rare genetic disorder with review of literature;Gopal;SAJ Case Report,2017
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1. Ocular manifestations and treatment progress of Crouzon syndrome;International Ophthalmology;2024-09-05
2. Genetics and the role it plays in craniofacial anomalies;Frontiers of Oral and Maxillofacial Medicine;2024-09
3. 3D computer-aided single stage correction of Crouzon related craniofacial and occlusal deformities: A case series of three adult patients;Oral and Maxillofacial Surgery Cases;2024-03
4. A unique presentation of Crouzon-like syndrome: Complex craniosynostosis in the absence of genetic mutations or familial predisposition – A case report;Surgical Neurology International;2023-12-08
5. Crouzon Syndrome Spanning Three Generations: Advances in the Treatment of Syndromic Midface Deficiency;Plastic and Reconstructive Surgery - Global Open;2023-11
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