Associated Papers
Screening for MSX1 and PAX9 gene variants among hypodontia patients in the Jordanian population.
Quran A et al.
Cellular and Molecular Biology (noisy-le-grand, France), 2026
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
Genotyping analysis of the Pax9 Gene in patients with maxillary canine impaction.
Vitria EE et al.
F1000research, 2019
WNT10A variants in relation to nonsyndromic hypodontia in eastern Slovak population.
Grejtakova D et al.
Journal of Genetics, 2018
A review on non-syndromic tooth agenesis associated with PAX9 mutations.
Fauzi NH et al.
The Japanese Dental Science Review, 2018
PAX9 gene mutations and tooth agenesis: A review.
Bonczek O et al.
Clinical Genetics, 2017
Mutational analysis of AXIN2, MSX1, and PAX9 in two Mexican oligodontia families.
Mu YD et al.
Genetics and Molecular Research : Gmr, 2013
PAX9 polymorphism and susceptibility to sporadic non-syndromic severe anodontia: a case-control study in southwest China.
Wang J et al.
Journal of Applied Oral Science : Revista Fob, 2013
Mutational analysis of MSX1 and PAX9 genes in Portuguese families with maxillary lateral incisor agenesis.
Pinho T et al.
European Journal of Orthodontics, 2010
Mutations in the PAX9 gene in sporadic oligodontia.
Pawlowska E et al.
Orthodontics & Craniofacial Research, 2010
A novel mutation in PAX9 causes familial form of molar oligodontia.
Mostowska A et al.
European Journal of Human Genetics : Ejhg, 2006
A novel c.581C>T transition localized in a highly conserved homeobox sequence of MSX1: is it responsible for oligodontia?
Mostowska A et al.
Journal of Applied Genetics, 2006
Identification of a nonsense mutation in the PAX9 gene in molar oligodontia.
Nieminen P et al.
European Journal of Human Genetics : Ejhg, 2001
Select a paper to view details