Associated Papers
Characterization of novel MSX1 variants causally associated with non-syndromic oligodontia in Chinese families.
Zhao Y et al.
Molecular Genetics & Genomic Medicine, 2024
38069551 (PubMed )
Supplement: MGG3-12-e2334-s002.xls › Sheet1
Next generation sequencing reveals a novel nonsense mutation in MSX1 gene related to oligodontia.
Bonczek O et al.
Plos One, 2018
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
Exclusion of PAX9 and MSX1 mutation in six families affected by tooth agenesis. A genetic study and literature review.
Tallón-Walton V et al.
Medicina Oral, Patologia Oral Y Cirugia Bucal, 2014
Tooth agenesis patterns and phenotype variation in a cohort of Belgian patients with hypodontia and oligodontia clustered in 79 families with their pedigrees.
Dreesen K et al.
European Journal of Orthodontics, 2014
Polymorphism in the MSX1 gene in a family with upper lateral incisor agenesis.
Boeira Junior BR et al.
Archives of Oral Biology, 2012
Novel nonsense mutation in MSX1 causes tooth agenesis with cleft lip in a Chinese family.
Liang J et al.
European Journal of Oral Sciences, 2012
Sequence analysis of PAX9, MSX1 and AXIN2 genes in a Chinese oligodontia family.
Wang J et al.
Archives of Oral Biology, 2011
A novel MSX1 mutation in hypodontia.
De Muynck S et al.
American Journal of Medical Genetics. Part A, 2004
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