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Article

Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone Development

1 May 1997

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9182764
DOI: 10.1016/s0092-8674(00)80259-7

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Cbfa1, a Candidate Gene for Cleidocranial Dysplasia Syndrome, Is Essential for Osteoblast Differentiation and Bone DevelopmentPMID 9182764Read ↗

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Role of Cbfa1 in osteoblast differentiation and functionSemantic proximity Read ↗

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A stop codon mutation in the CBFA 1 gene causes cleidocranial dysplasia.Semantic proximity Read ↗

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Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia.Semantic proximity Read ↗

Discovery: Osf2/Cbfa1, a master gene of bone formation.Semantic proximity Read ↗

Cbfa1 in bone development.Semantic proximity Read ↗

CBFA1 mutation analysis and functional correlation with phenotypic variability in cleidocranial dysplasia.Semantic proximity Read ↗

Cleidocranial dysplasia and RUNX2-clinical phenotype-genotype correlation.Semantic proximity Read ↗

Cleidocranial dysplasia: Clinical, endocrinologic and molecular findings in 15 patients from 11 familiesSemantic proximity Read ↗

RUNX2 mutations in cleidocranial dysplasiaSemantic proximity Read ↗

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