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A Case of Prader-Willi Syndrome with a Deletion Including MAGEL2, NDN, and MKRN3, but Excluding SNRPN and SNORD116.

Jannis Buecking,Yu An,Weimin Bi,Katrin Hinderhofer,Susanne Theiß,Anne Slavotinek,Christian P Schaaf

American journal of medical genetics Part A（2025）

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