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
Association of MSX1 Gene Variants with Nonsyndromic Cleft Lip and/or Palate in the Pakistani Population.
Memon A et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 2024
Genetic Factors of Teeth Impaction: Polymorphic and Haplotype Variants of PAX9, MSX1, AXIN2, and IRF6 Genes.
Trybek G et al.
International Journal of Molecular Sciences, 2023
Genetic and Morphological Variation in Hypodontia of Maxillary Lateral Incisors.
Kerekes-Máthé B et al.
Genes, 2023
MicroRNA-374a, -4680, and -133b suppress cell proliferation through the regulation of genes associated with human cleft palate in cultured human palate cells.
Suzuki A et al.
Bmc Medical Genomics, 2019
Genetic study of non-syndromic tooth agenesis through the screening of paired box 9, msh homeobox 1, axin 2, and Wnt family member 10A genes: a case-series.
Haddaji Mastouri M et al.
European Journal of Oral Sciences, 2018
Association of MSX1 c.*6C > T Variant with Nonsyndromic Cleft Lip With or Without Cleft Palate in Turkish Patients.
Aslar Oner D et al.
Genetic Testing and Molecular Biomarkers, 2016
Mutations in the MSX1 gene in Turkish children with non-syndromic tooth agenesis and other dental anomalies.
Ceyhan D et al.
Indian Journal of Dentistry, 2014
MSX1 mutation in witkop syndrome; a case report.
Ghaderi F et al.
Iranian Journal of Medical Sciences, 2013
Polymorphism in the MSX1 gene in a family with upper lateral incisor agenesis.
Boeira Junior BR et al.
Archives of Oral Biology, 2012
OTX2 mutations contribute to the otocephaly-dysgnathia complex.
Chassaing N et al.
Journal of Medical Genetics, 2012
MSX1 and orofacial clefting with and without tooth agenesis.
Modesto A et al.
Journal of Dental Research, 2006
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
Meta-analysis and systematic review for the genetic basis of cleft lip and palate.
Alghonemy WY et al.
Journal of Oral Biology and Craniofacial Research, 0