Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia. [PDF]
Gong L +10 more
europepmc +1 more source
Demographic, clinical, and radiological characteristics of cleidocranial dysplasia: A systematic review of cases reported in south America. [PDF]
Cano-Pérez E +4 more
europepmc +1 more source
Appropriateness of standard cephalometric norms for the assessment of dentofacial characteristics in patients with cleidocranial dysplasia. [PDF]
Savoldi F +5 more
europepmc +1 more source
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review. [PDF]
Thaweesapphithak S +4 more
europepmc +1 more source
Cleidocranial dysplasia: a case report and gene mutation analysis. [PDF]
Zhang P, He P, Xu P, Liao L.
europepmc +1 more source
Navigating challenges: Cleidocranial dysplasia and complexities in transvenous pacemaker implantation. [PDF]
El Ghiati H +8 more
europepmc +1 more source
Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis. [PDF]
Dalle Carbonare L +14 more
europepmc +1 more source
Three-dimensional evaluation of dental characteristics in patients with Cleidocranial dysplasia. [PDF]
Lu Y, Wang J, Li L, Zhang X.
europepmc +1 more source
Clinical and Radiological Insights of Cleidocranial Dysplasia: A Case Report of a Rare Medical Condition. [PDF]
Gowda Venkatesha RR +4 more
europepmc +1 more source
Familial Cleidocranial Dysplasia: A Diagnostic Challenge. [PDF]
Verma S, Koppula S, Kumar V.
europepmc +1 more source

