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. The National Academy of Sciences.
Citação norma ChicagoZhang, Yu-Wen, et al. A RUNX2/PEBP2αA/CBFA1 Mutation Displaying Impaired Transactivation and Smad Interaction in Cleidocranial Dysplasia. The National Academy of Sciences, 2000.
Citação norma MLAZhang, Yu-Wen, et al. A RUNX2/PEBP2αA/CBFA1 Mutation Displaying Impaired Transactivation and Smad Interaction in Cleidocranial Dysplasia. The National Academy of Sciences, 2000.
Nota: a formatação da citação pode não corresponder 100% ao definido pela respectiva norma.