Hyo-Jin Kim

The cleidocranial dysplasia‐related R131G mutation in the Runt‐related transcription factor RUNX2 disrupts binding to DNA but not CBF‐β

G. Stein, J. Lian, A. V. van Wijnen, 2010, Journal of cellular biochemistry.

Four novel RUNX2 mutations including a splice donor site result in the cleidocranial dysplasia phenotype

G. Stein, J. Lian, In‐San Kim, 2006, Journal of cellular physiology.