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