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.
Chicago Style citaatZhang, 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 citatieZhang, 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.
Let op: Deze citaties zijn niet altijd 100% accuraat.