Zhang, Y., Yasui, N., Ito, K., Huang, G., Fujii, M., Hanai, J., . . . Ito, Y. (2000). A RUNX2/PEBP2αA/CBFA1 mutation displaying impaired transactivation and Smad interaction in cleidocranial dysplasia. Proc Natl Acad Sci U S A.
Čikaški stil citiranjaZhang, Yu-Wen, et al. "A RUNX2/PEBP2αA/CBFA1 Mutation Displaying Impaired Transactivation and Smad Interaction in Cleidocranial Dysplasia." Proc Natl Acad Sci U S A 2000.
MLA način citiranjaZhang, Yu-Wen, et al. "A RUNX2/PEBP2αA/CBFA1 Mutation Displaying Impaired Transactivation and Smad Interaction in Cleidocranial Dysplasia." Proc Natl Acad Sci U S A 2000.
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