Evidence of intrafamilial variability of CBFA1/RUNX2 expression in cleidocranial dysplasia - A family study

Journal of Orofacial Orthopedics

Volumn 63, Issue 3, 2002, Pages 190-198

  Golan, Ilan ^a   Baumert, Uwe ^a   Wagener, Heinrich ^a   Preising, Markus ^a   Lorenz, Birgit ^a   Niederdellmann, Herbert ^a   Müßig, Dieter ^a  

^a UNIVERSITY OF REGENSBURG   (Germany)

Author keywords

Bone development; CBFA1 RUNX2; Cleidocranial dysplasia; Eburnization; Ossification

Indexed keywords

CORE BINDING FACTOR; TRANSCRIPTION FACTOR RUNX2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; CLEIDOCRANIAL DYSPLASIA; CLINICAL EXAMINATION; CLINICAL FEATURE; CONTROLLED STUDY; CRANIOFACIAL MALFORMATION; EXON; FAMILY STUDY; FATHER; GENE EXPRESSION; GENETIC ANALYSIS; GENETIC VARIABILITY; GENOTYPE; HUMAN; MALE; MISSENSE MUTATION; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; OSSIFICATION; PHENOTYPE; PRIORITY JOURNAL; SCHOOL CHILD; SIBLING; SYMPTOMATOLOGY; SYNDROME; TOOTH DISEASE;

ADULT; CEPHALOMETRY; CHILD; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; GENOTYPE; HUMANS; MALE; MUTATION, MISSENSE; NEOPLASM PROTEINS; PHENOTYPE; TRANSCRIPTION FACTORS; VARIATION (GENETICS);

EID: 0036263086     PISSN: 14345293     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00056-002-0123-4     Document Type: Article

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