Neonatal Familiar Cleidocranial Dysplasia: A Case Report. [PDF]
Zhao S, Wang T, Yang H, Huang R.
europepmc +1 more source
Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia. [PDF]
Gong L +10 more
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Demographic, clinical, and radiological characteristics of cleidocranial dysplasia: A systematic review of cases reported in south America. [PDF]
Cano-Pérez E +4 more
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Retinoblastoma binding protein-1 (RBP1) is a Runx2 coactivator and promotes osteoblastic differentiation [PDF]
David G Monroe +3 more
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Appropriateness of standard cephalometric norms for the assessment of dentofacial characteristics in patients with cleidocranial dysplasia. [PDF]
Savoldi F +5 more
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The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review. [PDF]
Thaweesapphithak S +4 more
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Cleidocranial dysplasia: a case report and gene mutation analysis. [PDF]
Zhang P, He P, Xu P, Liao L.
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Navigating challenges: Cleidocranial dysplasia and complexities in transvenous pacemaker implantation. [PDF]
El Ghiati H +8 more
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Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis. [PDF]
Dalle Carbonare L +14 more
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