Diversity of supernumerary tooth formation in siblings with cleidocranial dysplasia having identical mutation in RUNX2 : possible involvement of non-genetic or epigenetic regulation.

Suda, N; Hamada, T; Hattori, M; Torii, C; Kosaki, K; Moriyama, K

Suda, N; Hamada, T; Hattori, M; Torii, C; Kosaki, K; Moriyama, K.

Affiliation

Suda N; Department of Maxillofacial Reconstruction and Function, Division of Maxillofacial/Neck Reconstruction, Graduate School, Tokyo Medical and Dental University, Bunkyo-ku, Tokyo, Japan. n-suda.mort@tmd.ac.jp

Orthod Craniofac Res ; 10(4): 222-5, 2007 Nov.

Article in En | MEDLINE | ID: mdl-17973689

Subject(s)

Cleidocranial Dysplasia/complications; Core Binding Factor Alpha 1 Subunit/genetics; Tooth, Supernumerary/etiology; Adolescent; Amino Acid Substitution; Child; Cleidocranial Dysplasia/genetics; DNA Mutational Analysis; Epigenesis, Genetic; Female; Gene Expression Regulation, Developmental; Humans; Male; Mutation, Missense; Pedigree; Point Mutation; Siblings; Tooth, Supernumerary/genetics; Tooth, Supernumerary/pathology

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Collection: 01-internacional Database: MEDLINE Main subject: Tooth, Supernumerary / Cleidocranial Dysplasia / Core Binding Factor Alpha 1 Subunit Type of study: Prognostic_studies Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Orthod Craniofac Res Journal subject: ODONTOLOGIA / ORTODONTIA Year: 2007 Document type: Article Affiliation country: Japan

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