Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome - Eßinger, Carla; Karch, Stephanie; Moog, Ute; Fekete, György; Lengyel, Anna; Pinti, Eva; Eggermann, Thomas; Begemann, Matthias (Clinical epigenetics, 2020)
Gesehen am 23.06.2020