APA ציטוט

Capri, Y., Flex, E., Krumbach, O. H., Carpentieri, G., Cecchetti, S., Lißewski, C., . . . Zenker, M. (2019). Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome. Am J Hum Genet.

Citação norma Chicago

Capri, Yline, et al. "Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome." Am J Hum Genet 2019.

ציטוט MLA

Capri, Yline, et al. "Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome." Am J Hum Genet 2019.