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-Zitierstil (17. Ausg.)Eßinger, Carla, Stephanie Karch, Ute Moog, György Fekete, Anna Lengyel, Eva Pinti, Thomas Eggermann, und 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-Zitierstil (9. Ausg.)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.