Associated Papers
Genotype-phenotype pattern analysis of pathogenic PAX9 variants in Chinese Han families with non-syndromic oligodontia.
Ren J et al.
Frontiers in Genetics, 2023
37056289 (PubMed )
Supplement: Table1.XLSX › Sheet1
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
Familial oligodontia and regional odontodysplasia associated with a PAX9 initiation codon mutation.
Koskinen S et al.
Clinical Oral Investigations, 2019
A review on non-syndromic tooth agenesis associated with PAX9 mutations.
Fauzi NH et al.
The Japanese Dental Science Review, 2018
A novel G to A transition at initiation codon and exon-intron boundary of PAX9 identified in association with familial isolated oligodontia.
Sarkar T et al.
Gene, 2017
PAX9 gene mutations and tooth agenesis: A review.
Bonczek O et al.
Clinical Genetics, 2017
A novel initiation codon mutation of PAX9 in a family with oligodontia.
Liang J et al.
Archives of Oral Biology, 2016
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