Commentary on “Craniofacial Syndromes and class III phenotype: common genotype fingerprints? A scoping review and meta-analysis”
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Publisher
Springer Science and Business Media LLC
Link
https://www.nature.com/articles/s41390-024-03036-3.pdf
Reference10 articles.
1. Staudt, C. B. & Kiliaridis, S. Different skeletal types underlying Class III malocclusion in a random population. Am. J. Orthod. Dentofac. Orthop. 136, 715–721 (2009).
2. Zere, E., Chaudhari, P. K., Sharan, J., Dhingra, K. & Tiwari, N. Developing Class III malocclusions: challenges and solutions. Clin. Cosmet. Investig. Dent. 10, 99–116 (2018).
3. Gershater, E. et al. Genes and pathways associated with skeletal sagittal malocclusions: a systematic review. Int. J. Mol. Sci. 22, 13037 (2021).
4. Dehesa-Santos, A., Iber-Diaz, P. & Iglesias-Linares, A. Genetic factors contributing to skeletal class III malocclusion: a systematic review and meta-analysis. Clin. Oral. Investig. 25, 1587–1612 (2021).
5. Zohud, O. et al. Towards genetic dissection of skeletal Class III malocclusion: a review of genetic variations underlying the phenotype in humans and future directions. J. Clin. Med. 12, 3212 (2023).
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