The Phenotypes of Spheno-Occipital Synchondrosis in Patients With Crouzon Syndrome
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
General Medicine,Otorhinolaryngology,Surgery
Reference21 articles.
1. Apert and Crouzon syndromes: clinical findings, genes and extracellular matrix;Carinci;J Craniofac Surg,2005
2. Clinical features of Crouzon's syndrome patients with and without a positive family history of Crouzon's syndrome;al-Qattan;J Craniofac Surg,1997
3. FGFR2 mutations among Thai children with Crouzon and Apert syndromes;Shotelersuk;J Craniofac Surg,2003
4. Germline and somatic mosaicism for FGFR2 mutation in the mother of a child with Crouzon syndrome: implications for genetic testing in “paternal age-effect” syndromes;Goriely;Am J Med Genet A,2010
5. Cranial base in craniofacial development: developmental features, influence on facial growth, anomaly, and molecular basis;Nie;Acta Odontol Scand,2005
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1. Timing of Spheno-Occipital Synchondrosis Closure in Cleft Lip and Palate Patients in Iranian Population;The Cleft Palate-Craniofacial Journal;2022-04-06
2. The Interchondral Joints of Thorax in Microtia Surgery;Annals of Plastic Surgery;2021-02-01
3. Radiological Investigations of Craniofacial Malformations;Fundamentals of Craniofacial Malformations;2021
4. Postnatal Development of the Spheno-occipital Synchondrosis;Journal of Craniofacial Surgery;2017-09
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