APA (7th ed.) Citation

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. Clinical epigenetics, 12(1), . https://doi.org/10.1186/s13148-020-00856-y

Chicago Style (17th ed.) Citation

Eßinger, Carla, Stephanie Karch, Ute Moog, György Fekete, Anna Lengyel, Eva Pinti, Thomas Eggermann, and Matthias Begemann. "Frequency of KCNQ1 Variants Causing Loss of Methylation of Imprinting Centre 2 in Beckwith-Wiedemann Syndrome." Clinical Epigenetics 12, no. 1 (2020). https://doi.org/10.1186/s13148-020-00856-y.

MLA (9th ed.) Citation

Eßinger, Carla, et al. "Frequency of KCNQ1 Variants Causing Loss of Methylation of Imprinting Centre 2 in Beckwith-Wiedemann Syndrome." Clinical Epigenetics, vol. 12, no. 1, 2020, https://doi.org/10.1186/s13148-020-00856-y.