Associated Papers
Molecular-based phenotype variations in amelogenesis imperfecta.
Dong J et al.
Oral Diseases, 2023
Novel ITGB6 variants cause hypoplastic-hypomineralized amelogenesis imperfecta and taurodontism: characterization of tooth phenotype and review of literature.
Sriwattanapong K et al.
Bdj Open, 2023
Novel ITGB6 mutation in autosomal recessive amelogenesis imperfecta.
Seymen F et al.
Oral Diseases, 2015
Select a paper to view details