Advances in the molecular pathogenesis of craniofacial conditions
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology,Oral Surgery,Surgery
Reference153 articles.
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2. Spectrum of craniosynostosis phenotypes associated with novel mutations at the fibroblast growth factor receptor 2 locus;Pulleyn;Eur J Hum Genet,1996
3. A unique point mutation in the fibroblast growth factor receptor 3 gene (FGFR3) defines a new craniosynostosis syndrome;Muenke;Am J Hum Genet,1997
4. FGFR2 mutation in clinically nonclassifiable autosomal dominant craniosynostosis with pronounced phenotypic variation;Steinberger;Am J Med Genet,1996
5. Craniosynostosis, midfacial hypoplasia and foot abnormalities: an autosomal dominant phenotype in a large Amish kindred;Jackson;J Pediatr,1976
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1. Craniofacial Surgery for Congenital and Acquired Deformities;Cummings Pediatric Otolaryngology;2021
2. Evaluating the Efficacy of Monobloc Distraction in the Crouzon-Pfeiffer Craniofacial Deformity Using Geometric Morphometrics;Plastic and Reconstructive Surgery;2017-02
3. Craniosynostosis;Plastic and reconstructive surgery;2015-03-27
4. Craniofacial Surgery for Congenital and Acquired Deformities;Cummings Pediatric Otolaryngology;2015
5. Long-term surgical cure of severe obstructive sleep apnea in an adult patient with craniofacial dysostosis (Crouzon’s syndrome): a case report and literature review;Sleep and Breathing;2010-08-26
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