A natural history of cleidocranial dysplasia

American Journal of Medical Genetics

Volumn 104, Issue 1, 2001, Pages 1-6

  Zappella, Michele ^a   Meloni, Ilaria ^b   Longo, Ilaria ^b   Hayek, Giuseppe ^a   Renieri, Alessandra ^b  

^a Azienda Ospedaliera   (Italy)

^b UNIVERSITY OF SIENA   (Italy)

Author keywords

Autosomal dominant; Bone; CBFA1; Cleidocranial dysostosis; Dental abnormalities; Skeletal dysplasia

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR RUNX2; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BONE DYSPLASIA; CELL DIFFERENTIATION; CHILD; CLEIDOCRANIAL DYSPLASIA; CLINICAL FEATURE; CONTROLLED STUDY; FEMALE; FLATFOOT; GENE MUTATION; HEARING LOSS; HUMAN; MAJOR CLINICAL STUDY; MALE; OSTEOBLAST; OTITIS MEDIA; PRIORITY JOURNAL; SCOLIOSIS; TOOTH DISEASE; UPPER RESPIRATORY TRACT INFECTION; VALGUS KNEE;

ADOLESCENT; ADULT; CESAREAN SECTION; CHILD; CHILD, PRESCHOOL; CLEIDOCRANIAL DYSPLASIA; FEMALE; FLATFOOT; HEARING LOSS; HUMANS; MALE; MALOCCLUSION; MUSCULOSKELETAL ABNORMALITIES; PEDIGREE; PREGNANCY; RESPIRATORY SYSTEM ABNORMALITIES; SCOLIOSIS; TOOTH ABNORMALITIES; TOOTH ERUPTION; TOOTH, SUPERNUMERARY;

EID: 0035889364     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10024     Document Type: Article

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