Ogawa S, Higuchi S, Yoshimoto Y, Hoshino M, Miura S, Hamada A, Watanabe H, Sakuma T, Hu K, Ogata S, Uchibe K, Fujimoto K, Yamamoto T, Okamoto T, Kunimatsu R, Sotomaru Y, Tanimoto K, Kondoh G, Komori T, Docheva D, Shukunami C. Functional impact of pathogenic mutations in the Runt homology domain of mouse Runx2 on skeletal and dental phenotypes in cleidocranial dysplasia Journal of Bone and Mineral Research. 2025.12; ( PubMed, DOI )