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
A Synonymous Exonic Splice Silencer Variant in IRF6 as a Novel and Cryptic Cause of Non-Syndromic Cleft Lip and Palate.
Sylvester B et al.
Genes, 2020
A novel mutation of MSX1 inherited from maternal mosaicism causes a severely affected child with nonsyndromic oligodontia.
Ma T et al.
Annals of Human Genetics, 2020
Two novel mutations in MSX1 causing oligodontia.
Yang L et al.
Plos One, 2020
31914153 (PubMed )
Supplement: pone.0227287.s007.docx
TGFβ3, MSX1, and MMP3 as Candidates for NSCL±P in an Indian Population.
Kumari P et al.
The Cleft Palate-craniofacial Journal : Official Publication of the American Cleft Palate-craniofacial Association, 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
Clinical and genetic evaluation of a Chinese family with isolated oligodontia.
Qin H et al.
Archives of Oral Biology, 2013
Select a paper to view details