Concomitant 11p15.4‐p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith–Wiedemann syndrome. Issue 12 (23rd August 2016) - Peterson, Jess F.; Bick, David P.; Geddes, Gabrielle C.; McCarrier, Julie; Grignon, John W.; Chirempes, Brett; Broeckel, Ulrich; Abidi, Fatima; Rogers, Richard C.; Boccuto, Luigi; DuPont, Barbara; vanTuinen, Peter