Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia

Orthodontics and Craniofacial Research

Volumn 13, Issue 4, 2010, Pages 197-202

  Suda, N ^a   Hattori, M ^a   Kosaki, K ^b   Banshodani, A ^c   Kozai, K ^c   Tanimoto, K ^c   Moriyama, K ^a  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^b KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c HIROSHIMA UNIVERSITY   (Japan)

Author keywords

Cleidocranial dysplasia; Gene mutation; RUNX2; Supernumerary tooth

Indexed keywords

ADENINE; ARGININE; GLUTAMINE; PROLINE; RUNX2 PROTEIN, HUMAN; SERINE; THYMINE; TRANSCRIPTION FACTOR RUNX2;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLEIDOCRANIAL DYSPLASIA; COPY NUMBER VARIATION; FEMALE; FRAMESHIFT MUTATION; GENE EXPRESSION REGULATION; GENETIC EPIGENESIS; GENETIC HETEROGENEITY; GENETIC VARIABILITY; GENETICS; GENOTYPE; HUMAN; MALE; MIDDLE AGED; MISSENSE MUTATION; MONOZYGOTIC TWINS; MUTATION; POINT MUTATION; TOOTH MALFORMATION; TWINS;

ADENINE; ADOLESCENT; ADULT; ARGININE; CHILD; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; DISEASES IN TWINS; DNA COPY NUMBER VARIATIONS; EPIGENESIS, GENETIC; FEMALE; FRAMESHIFT MUTATION; GENETIC HETEROGENEITY; GENETIC VARIATION; GENOTYPE; GLUTAMINE; HUMANS; MALE; MIDDLE AGED; MUTAGENESIS, INSERTIONAL; MUTATION; MUTATION, MISSENSE; POINT MUTATION; PROLINE; SERINE; THYMINE; TOOTH, SUPERNUMERARY; TWINS, MONOZYGOTIC;

EID: 77958089507     PISSN: 16016335     EISSN: 16016343     Source Type: Journal    
DOI: 10.1111/j.1601-6343.2010.01495.x     Document Type: Article

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