Isolated oligodontia associated with mutations in EDARADD, AXIN2, MSX1, and PAX9 genes
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.34045/fullpdf
Reference42 articles.
1. Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia;Azeem;Arch Dermatol Res,2009
2. The genetic basis of inherited anomalies of the teeth. Part 1: Clinical and molecular aspects of non-syndromic dental disorders;Bailleul-Forestier;Eur J Med Genet,2008a
3. The genetic basis of inherited anomalies of the teeth. Part 2: Syndromes with significant dental involvement;Bailleul-Forestier;Eur J Med Genet,2008b
4. Signs and symptoms from ectodermal organs in young Swedish individuals with oligodontia;Bergendal;Int J Paediatr Dent,2006
5. Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis;Callahan;Arch Oral Biol,2009
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1. The oligodontia phenotype in a X-linked hypohidrotic ectodermal dysplasia patient with a novel EVC2 variant;Heliyon;2024-01
2. Characterization of novel MSX1 variants causally associated with non‐syndromic oligodontia in Chinese families;Molecular Genetics & Genomic Medicine;2023-12-08
3. Insights in orthodontic genetic and epigenetic knowledge and its translation in clinical practice;Seminars in Orthodontics;2023-09
4. A novel pathogenic frameshift variant in AXIN2 in a man with polyposis and hypodontia;Hereditary Cancer in Clinical Practice;2023-08-25
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