The phenotype and genotype of PAX9 mutations causing tooth agenesis
Author:
Publisher
Springer Science and Business Media LLC
Subject
General Dentistry
Link
https://link.springer.com/content/pdf/10.1007/s00784-023-05056-5.pdf
Reference21 articles.
1. Ross JN, Ruigrok LC, Fennis WMM, Cune MS, Rosenberg A, van Nunen AB et al (2021) Gastrointestinal symptoms in patients with isolated oligodontia and a Wnt gene mutation. Oral Dis. https://doi.org/10.1111/odi.13954
2. De Santis D, Sinigaglia S, Faccioni P, Pancera P, Luciano U, Bertossi D et al (2019) Syndromes associated with dental agenesis. Minerva Stomatol 68(1):42–56. https://doi.org/10.23736/S0026-4970.18.04129-8
3. Ye X, Attaie AB (2016) Genetic basis of nonsyndromic and syndromic tooth agenesis. J Pediatr Genet 5(4):198–208. https://doi.org/10.1055/s-0036-1592421
4. Gracco ALT, Zanatta S, ForinValvecchi F, Bignotti D, Perri A, Baciliero F (2017) Prevalence of dental agenesis in a sample of Italian orthodontic patients: an epidemiological study. Prog Orthod 18(1):33. https://doi.org/10.1186/s40510-017-0186-9
5. Zhao K, Lian M, Zou D, Huang W, Zhou W, Shen Y et al (2019) Novel mutations identified in patients with tooth agenesis by whole-exome sequencing. Oral Dis 25(2):523–534. https://doi.org/10.1111/odi.13002
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