Revisiting Wilms tumour surveillance in Beckwith-Wiedemann syndrome with IC2 methylation loss, reply.
Fréderic BrioudeRaoul HennekamJet BliekCarole CozeThomas EggermannGiovanni B FerreroChristian KratzYves Le BoucSaskia M MaasDeborah J G MackayEamonn R MaherAlessandro MussaIrene NetchinePublished in: European journal of human genetics : EJHG (2018)