Cite
WHOLE EXOME SEQUENCING IDENTIFIED THAT THE MAPK AND PI3K PATHWAYS ARE THE MAIN TARGETS FOR MUTATIONS IN INTRACRANIAL GERM CELL TUMORS.
MLA
Ichimura, Koichi, et al. “Whole Exome Sequencing Identified That the Mapk and Pi3k Pathways Are the Main Targets for Mutations in Intracranial Germ Cell Tumors.” Neuro-Oncology, vol. 16, no. suppl_3, July 2014, p. iii23. EBSCOhost, widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edb&AN=97675660&authtype=sso&custid=ns315887.
APA
Ichimura, K., Fukushima, S., Totoki, Y., Matsushita, Y., Otsuka, A., Tomiyama, A., Niwa, T., Sakai, R., Ushijima, T., Nakamura, T., Suzuki, T., Fukuoka, K., Yanagisawa, T., Mishima, K., Nakazato, Y., Hosoda, F., Narita, Y., Shibui, S., Yoshida, A., & Takami, H. (2014). Whole Exome Sequencing Identified That the Mapk and Pi3k Pathways Are the Main Targets for Mutations in Intracranial Germ Cell Tumors. Neuro-Oncology, 16(suppl_3), iii23.
Chicago
Ichimura, Koichi, Shintaro Fukushima, Yasushi Totoki, Yuko Matsushita, Ayaka Otsuka, Arata Tomiyama, Tohru Niwa, et al. 2014. “Whole Exome Sequencing Identified That the Mapk and Pi3k Pathways Are the Main Targets for Mutations in Intracranial Germ Cell Tumors.” Neuro-Oncology 16 (suppl_3): iii23. http://widgets.ebscohost.com/prod/customlink/proxify/proxify.php?count=1&encode=0&proxy=&find_1=&replace_1=&target=https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&scope=site&db=edb&AN=97675660&authtype=sso&custid=ns315887.