Cleidocranial dysplasia and novel RUNX2 variants: dental, craniofacial, and osseous manifestations. [PDF]
Thaweesapphithak S +5 more
europepmc +1 more source
Neonatal Familiar Cleidocranial Dysplasia: A Case Report. [PDF]
Zhao S, Wang T, Yang H, Huang R.
europepmc +1 more source
A Chinese premature infant with cleidocranial dysplasia characterized by heterozygous RUNX2 mutation and cerebral infarction: a case report. [PDF]
Zhao W +5 more
europepmc +1 more source
Cleidocranial Dysplasia With Multiple Impacted Teeth and Dentigerous Cysts: A Case Report of a Rare Entity. [PDF]
Shinh M.
europepmc +1 more source
A Cryptic CBFB Deletion-Inversion Expands the Mutational Spectrum of Variants Associated With Cleidocranial Dysplasia. [PDF]
Pagnamenta AT +6 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
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

