Cleidocranial dysplasia: Oral features and genetic analysis of 11 patients

Oral Diseases

Volumn 18, Issue 2, 2012, Pages 184-190

  Bufalino, A ^a   Paranaiba L M R ^a,b   Gouvea A F ^a   Gueiros, L A ^c   Martelli Junior H ^b   Junior, J J ^a   Lopes, M A ^a   Graner, E ^a   de Almeida, O P ^a   Vargas, P A ^a   Coletta, R D ^a  

^a UNIVERSITY OF CAMPINAS   (Brazil)

^b STATE UNIVERSITY OF MONTES CLAROS   (Brazil)

^c FEDERAL UNIVERSITY OF PERNAMBUCO   (Brazil)

Author keywords

Cleidocranial dysplasia; Dental abnormalities; Mutation; RUNX2

Indexed keywords

TRANSCRIPTION FACTOR RUNX2;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLEIDOCRANIAL DYSPLASIA; CLINICAL ARTICLE; CORRELATION ANALYSIS; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENOTYPE; HUMAN; MALE; MALOCCLUSION; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRESCHOOL CHILD; PRIORITY JOURNAL; TOOTH DISEASE; TOOTH MALFORMATION;

ADOLESCENT; ADULT; CHILD; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; DNA MUTATIONAL ANALYSIS; FEMALE; FRAMESHIFT MUTATION; GENES, DOMINANT; HETEROZYGOTE; HUMANS; MALE; MALOCCLUSION; MUTATION, MISSENSE; PEDIGREE; PROTEIN STRUCTURE, TERTIARY; TOOTH, IMPACTED; TOOTH, SUPERNUMERARY; YOUNG ADULT;

EID: 84855920933     PISSN: 1354523X     EISSN: 16010825     Source Type: Journal    
DOI: 10.1111/j.1601-0825.2011.01862.x     Document Type: Article

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