Oral features in Apert syndrome: a histological investigation

Author:

Surman TL,Logan RM,Townsend GC,Anderson PJ

Publisher

Wiley

Subject

Otorhinolaryngology,Oral Surgery,Surgery,Orthodontics

Reference24 articles.

1. Two specimens of congenital cranial deformity in infants associated with fusion of fingers and toes;Wheaton;Trans Pathol Soc Lond,1894

2. De L’acrocephalosyndactylie;Apert;Bull Mem Soc Med Hop Paris,1906

3. Birth prevalence, mutation rate, sex ration, parent’s age, and ethnicity in Apert syndrome;Tolarova;Am J Med Genet,1997

4. Fibroblast growth factors, their receptors and receptor disorders;Gorlin;J Craniomaxillofac Surg,1997

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1. Unraveling the Complexity of Apert Syndrome: Genetics, Clinical Insights, and Future Frontiers;Cureus;2023-10-18

2. The Benefits of CBCT Imaging in the Diagnosis of Individuals with Craniofacial Anomalies;Journal of the California Dental Association;2023-08-24

3. Dental, Occlusal, and Functional Evaluation of Patients;Fundamentals of Craniofacial Malformations;2023

4. Diagnosis of Dentofacial Anomolies;Rare Diseases - Recent Advances [Working Title];2022-11-03

5. Apert Syndrome: Dental management considerations and objectives;Journal of Oral Biology and Craniofacial Research;2022-05

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