Trích dẫn APA

Eßinger, C., Karch, S., Moog, U., Fekete, G., Lengyel, A., Pinti, E., . . . Begemann, M. (2020). Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome. Clin Epigenetics.

Trích dẫn kiểu Chicago

Eßinger, Carla, Stephanie Karch, Ute Moog, György Fekete, Anna Lengyel, Eva Pinti, Thomas Eggermann, và Matthias Begemann. "Frequency of KCNQ1 Variants Causing Loss of Methylation of Imprinting Centre 2 in Beckwith-Wiedemann Syndrome." Clin Epigenetics 2020.

Trích dẫn MLA

Eßinger, Carla, et al. "Frequency of KCNQ1 Variants Causing Loss of Methylation of Imprinting Centre 2 in Beckwith-Wiedemann Syndrome." Clin Epigenetics 2020.

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