Associated Papers
Tooth agenesis patterns and variants in PAX9: A systematic review.
Intarak N et al.
The Japanese Dental Science Review, 2023
37159578 (PubMed )
Supplement: mmc1.docx
The phenotype and genotype of PAX9 mutations causing tooth agenesis.
Jiang C et al.
Clinical Oral Investigations, 2023
Genotype-phenotype pattern analysis of pathogenic PAX9 variants in Chinese Han families with non-syndromic oligodontia.
Ren J et al.
Frontiers in Genetics, 2023
Four Novel PAX9 Variants and the PAX9-Related Non-Syndromic Tooth Agenesis Patterns.
Liu H et al.
International Journal of Molecular Sciences, 2022
35897718 (PubMed )
Supplement: ijms-23-08142-s001.zip › ijms-1830351-supplementary.pdf
The role of PAX9 promoter gene polymorphisms in causing hypodontia: a study in the Jordanian population.
Abu-Siniyeh A et al.
The Application of Clinical Genetics, 2018
Characterization of a novel mutation in PAX9 gene in a family with non-syndromic dental agenesis.
Haddaji Mastouri M et al.
Archives of Oral Biology, 2016
A novel initiation codon mutation of PAX9 in a family with oligodontia.
Liang J et al.
Archives of Oral Biology, 2016
Novel PAX9 mutations cause non-syndromic tooth agenesis.
Mitsui SN et al.
Journal of Dental Research, 2014
Novel PAX9 mutation associated with syndromic tooth agenesis.
Mostowska A et al.
European Journal of Oral Sciences, 2013
Mutations in WNT10A are present in more than half of isolated hypodontia cases.
van den Boogaard MJ et al.
Journal of Medical Genetics, 2012
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