Atypical expression of cleidocranial dysplasia: Clinical and molecular-genetic analysis

Orthodontics and Craniofacial Research

Volumn 5, Issue 4, 2002, Pages 243-249

  Golan, I ^a   Baumert, U ^a   Muss D ^a   Wagener, H ^a   Niederdellmann, H ^a   Dauwerse, J ^b   Preising, M ^a   Lorenz, B ^a  

^a UNIVERSITY OF REGENSBURG   (Germany)

^b LEIDEN UNIVERSITY   (Netherlands)

Author keywords

CBFA1; Eburnisation; Rubinstein taybi syndrome

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX2; TUMOR PROTEIN;

ADOLESCENT; ARTICLE; CASE REPORT; CEPHALOMETRY; CLEIDOCRANIAL DYSPLASIA; DIAGNOSTIC ERROR; DIFFERENTIAL DIAGNOSIS; FACIES; FLUORESCENCE IN SITU HYBRIDIZATION; GENETICS; HUMAN; MALE; MISSENSE MUTATION; PATHOLOGY; RUBINSTEIN SYNDROME; SINGLE STRAND CONFORMATION POLYMORPHISM;

ADOLESCENT; CEPHALOMETRY; CLEIDOCRANIAL DYSPLASIA; CORE BINDING FACTOR ALPHA 1 SUBUNIT; DIAGNOSIS, DIFFERENTIAL; DIAGNOSTIC ERRORS; FACIES; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; MALE; MUTATION, MISSENSE; NEOPLASM PROTEINS; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RUBINSTEIN-TAYBI SYNDROME; TRANSCRIPTION FACTORS;

EID: 0036832573     PISSN: 16016335     EISSN: 16016343     Source Type: Journal    
DOI: 10.1034/j.1600-0544.2002.02206.x     Document Type: Article

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