A case of Prader-Willi syndrome with a deletion including MAGEL2 , NDN , and MKRN3 , but excluding SNRPN and SNORD116 - Bücking, Jannis; An, Yu; Bi, Weimin; Hinderhofer, Katrin; Theiß, Susanne; Slavotinek, Anne; Schaaf, Christian P. (American journal of medical genetics, 2025)
Veröffentlicht: 15 April 2025