Results 141 to 150 of about 3,948 (205)

Identification a novel de novo RUNX2 frameshift mutation associated with cleidocranial dysplasia. [PDF]

open access: yesGenes Genomics, 2022
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]

open access: yesAnn Med Surg (Lond), 2022
Cano-Pérez E   +4 more
europepmc   +1 more source

The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review. [PDF]

open access: yesJ Transl Med
Thaweesapphithak S   +4 more
europepmc   +1 more source

Cleidocranial dysplasia: a case report and gene mutation analysis. [PDF]

open access: yesHua Xi Kou Qiang Yi Xue Za Zhi, 2022
Zhang P, He P, Xu P, Liao L.
europepmc   +1 more source

Navigating challenges: Cleidocranial dysplasia and complexities in transvenous pacemaker implantation. [PDF]

open access: yesRadiol Case Rep
El Ghiati H   +8 more
europepmc   +1 more source

Unraveling RUNX2 mutation in a cleidocranial dysplasia patient: Molecular insights into osteogenesis and proteostasis. [PDF]

open access: yesGenes Dis
Dalle Carbonare L   +14 more
europepmc   +1 more source

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