APA aipamena

Miyatake, S., Okamoto, N., Stark, Z., Nabetani, M., Tsurusaki, Y., Nakashima, M., . . . Matsumoto, N. (2017). ANKRD11 variants cause variable clinical features associated with KBG syndrome and Coffin–Siris-like syndrome. J Hum Genet.

Chicago Style aipamena

Miyatake, Satoko, et al. "ANKRD11 Variants Cause Variable Clinical Features Associated With KBG Syndrome and Coffin–Siris-like Syndrome." J Hum Genet 2017.

MLA aipamena

Miyatake, Satoko, et al. "ANKRD11 Variants Cause Variable Clinical Features Associated With KBG Syndrome and Coffin–Siris-like Syndrome." J Hum Genet 2017.