Associated Papers
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
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
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