APA
Tsuchida N., Nakashima M., Kato M., Heyman E., Inui T., Haginoya K., Watanabe S., Chiyonobu T., Morimoto M., Ohta M., Kumakura A., Kubota M., Kumagai Y., Hamano S., Lourenco C. M., Yahaya N. A., Ch'ng G., Ngu L., Fattal-Valevski A., Weisz Hubshman M., Orenstein N., Marom D., Cohen L., Goldberg-Stern H., Uchiyama Y., Imagawa E., Mizuguchi T., Takata A., Miyake N., Nakajima H., Saitsu H., Miyatake S. & Matsumoto N. (20190911). Detection of copy number variations in epilepsy using exome data. : Clinical genetics.
Chicago
Tsuchida N, Nakashima M, Kato M, Heyman E, Inui T, Haginoya K, Watanabe S, Chiyonobu T, Morimoto M, Ohta M, Kumakura A, Kubota M, Kumagai Y, Hamano S-I, Lourenco C M, Yahaya N A, Ch'ng G-S, Ngu L-H, Fattal-Valevski A, Weisz Hubshman M, Orenstein N, Marom D, Cohen L, Goldberg-Stern H, Uchiyama Y, Imagawa E, Mizuguchi T, Takata A, Miyake N, Nakajima H, Saitsu H, Miyatake S and Matsumoto N. 20190911. Detection of copy number variations in epilepsy using exome data. : Clinical genetics.
Harvard
Tsuchida N., Nakashima M., Kato M., Heyman E., Inui T., Haginoya K., Watanabe S., Chiyonobu T., Morimoto M., Ohta M., Kumakura A., Kubota M., Kumagai Y., Hamano S., Lourenco C. M., Yahaya N. A., Ch'ng G., Ngu L., Fattal-Valevski A., Weisz Hubshman M., Orenstein N., Marom D., Cohen L., Goldberg-Stern H., Uchiyama Y., Imagawa E., Mizuguchi T., Takata A., Miyake N., Nakajima H., Saitsu H., Miyatake S. and Matsumoto N. (20190911). Detection of copy number variations in epilepsy using exome data. : Clinical genetics.
MLA
Tsuchida N, Nakashima M, Kato M, Heyman E, Inui T, Haginoya K, Watanabe S, Chiyonobu T, Morimoto M, Ohta M, Kumakura A, Kubota M, Kumagai Y, Hamano S-I, Lourenco C M, Yahaya N A, Ch'ng G-S, Ngu L-H, Fattal-Valevski A, Weisz Hubshman M, Orenstein N, Marom D, Cohen L, Goldberg-Stern H, Uchiyama Y, Imagawa E, Mizuguchi T, Takata A, Miyake N, Nakajima H, Saitsu H, Miyatake S and Matsumoto N. Detection of copy number variations in epilepsy using exome data. : Clinical genetics. 20190911.