Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome

Eßinger, Carla; Karch, Stephanie; Moog, Ute; Fekete, György [Fekete, György (Gyermekgyógyászat...), author] II. Department of Pediatrics (SU / FM / C); Lengyel, Anna [Lengyel, Anna (gyermekgyógyászat), author] II. Department of Pediatrics (SU / FM / C); Pinti, Eva [Pinti, Éva (klinikai genetika), author] II. Department of Pediatrics (SU / FM / C); Eggermann, Thomas ✉; Begemann, Matthias