Craniofacial microsomia – more than a structural malformation
Author:
Affiliation:
1. Pediatric Dentistry and Orthodontics, Institute of Dentistry University of Turku Turku Finland
2. Department of Community Dentistry, Institute of Dentistry University of Turku Turku Finland
Publisher
Wiley
Subject
Otorhinolaryngology,Oral Surgery,Surgery,Orthodontics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ocr.12592
Reference27 articles.
1. Atlas of Genetic Diagnosis and Counseling
2. Craniofacial Microsomia
3. Oculo-auriculo-vertebral spectrum: a review of the literature and genetic update
4. An association between hemifacial microsomia and facial clefting
5. Dental anomalies in craniofacial microsomia: A systematic review
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1. FBLN2 is associated with Goldenhar syndrome and is essential for cranial neural crest cell development;Annals of the New York Academy of Sciences;2024-07
2. Functional and Genetic Analyses Unveil the Implication of CDC27 in Hemifacial Microsomia;International Journal of Molecular Sciences;2024-04-26
3. Clinical report and genetic analysis of a Chinese neonate with craniofacial microsomia caused by a splicing variant of the splicing factor 3b subunit 2 gene;Molecular Genetics & Genomic Medicine;2023-08-09
4. Establishing an International Interdisciplinary Research Network in Craniofacial Microsomia: The CARE Program;The Cleft Palate Craniofacial Journal;2023-05-29
5. Orthodontic considerations for patients presenting with Goldenhar Syndrome: A long-term case report;Australasian Orthodontic Journal;2023-01-01
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