Associated Papers
The impact of RUNX2 gene variants on cleidocranial dysplasia phenotype: a systematic review.
Thaweesapphithak S et al.
Journal of Translational Medicine, 2024
39627759 (PubMed )
Supplement: 12967_2024_5904_MOESM1_ESM.xlsx › Supplement_table_1.
A novel RUNX2 splice site mutation in Chinese associated with cleidocranial dysplasia.
Wang J et al.
Heliyon, 2024
Functional analysis of novel RUNX2 mutations identified in patients with cleidocranial dysplasia.
Hordyjewska-Kowalczyk E et al.
Clinical Genetics, 2019
Identification of a novel RUNX2 gene mutation in an Italian family with cleidocranial dysplasia.
Marchisella C et al.
European Journal of Orthodontics, 2011
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