Oral Findings in a Typical Case of Achondroplasia
Author:
Affiliation:
1. Department of Oral Diagnosis and Maxillofacial Radiology, Ondokuz Mayis University, Samsun, Turkey
2. Department of Orthodontics, Ondokuz Mayis University, Samsun, Turkey
3. Department of Radiodiagnostics, Ondokuz Mayis University, Samsun, Turkey
Abstract
Publisher
SAGE Publications
Subject
Biochemistry, medical,Cell Biology,Biochemistry,General Medicine
Link
http://journals.sagepub.com/doi/pdf/10.1177/147323000303100311
Reference7 articles.
1. Mutations in the transmembrane domain of FGFR3 cause the most common genetic form of dwarfism, achondroplasia
2. Dental anomalies in association with achondroplasia. Report of two cases
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