A <Emphasis Type="Italic">RUNX2/PEBP2αA/CBFA1</Emphasis> mutation in cleidocranial dysplasia revealing the link between the gene and Smad.[J].Yoshiaki Ito;Yu-Wen Zhang.Journal of Bone and Mineral Metabolism.2001, 3
A <Emphasis Type="Italic">RUNX2/PEBP2αA/CBFA1</Emphasis> mutation in cleidocranial dysplasia revealing the link between the gene and Smad.[J].Yoshiaki Ito;Yu-Wen Zhang.Journal of Bone and Mineral Metabolism.2001, 3