An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome
Izuho Hatada(National Cerebral and Cardiovascular Center), Tsunehiro Mukai(Nishikyushu University), Hirofumi Ohashi(Saitama Children's Medical Center), Akira Nabetani(National Cerebral and Cardiovascular Center), Akira Okada(The University of Osaka), Hiroko Morisaki(National Cerebral and Cardiovascular Center), Yoshimitsu Fukushima(Saitama Children's Medical Center), Masahiro Inoue(Osaka University), Yasuhiko Kaneko(MRC Laboratory of Molecular Biology), Yosuke Komoto(The University of Osaka), Masahiro Nakayama(Osaka International Cancer Institute), Norio Niikawa(Nagasaki University), Sachiko Oh‐ishi(National Cerebral and Cardiovascular Center)
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