APA

Fu X. J., Morisada N., Hashimoto F., Taniguchi-Ikeda M., Hashimura Y., Ohtsubo H., Ninchoji T., Kaito H., Nozu K., Takahashi E., Nakanishi K., Kurahashi H. & Iijima K. (20160415). A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy. : Human genome variation.

Chicago

Fu Xue J, Morisada Naoya, Hashimoto Fusako, Taniguchi-Ikeda Mariko, Hashimura Yuya, Ohtsubo Hiromi, Ninchoji Takeshi, Kaito Hiroshi, Nozu Kandai, Takahashi Eihiko, Nakanishi Koichi, Kurahashi Hiroki and Iijima Kazumoto. 20160415. A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy. : Human genome variation.

Harvard

Fu X. J., Morisada N., Hashimoto F., Taniguchi-Ikeda M., Hashimura Y., Ohtsubo H., Ninchoji T., Kaito H., Nozu K., Takahashi E., Nakanishi K., Kurahashi H. and Iijima K. (20160415). A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy. : Human genome variation.

MLA

Fu Xue J, Morisada Naoya, Hashimoto Fusako, Taniguchi-Ikeda Mariko, Hashimura Yuya, Ohtsubo Hiromi, Ninchoji Takeshi, Kaito Hiroshi, Nozu Kandai, Takahashi Eihiko, Nakanishi Koichi, Kurahashi Hiroki and Iijima Kazumoto. A patient with autosomal recessive Alport syndrome due to segmental maternal isodisomy. : Human genome variation. 20160415.