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An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndrome

✍ Scribed by Hatada, Izuho; Ohashi, Hirofumi; Fukushima, Yoshimitsu; Kaneko, Yasuhiko; Inoue, Masahiro; Komoto, Yosuke; Okada, Akira; Ohishi, Sachiko; Nabetani, Akira; Morisaki, Hiroko


Book ID
109918296
Publisher
Nature Publishing Group
Year
1996
Tongue
English
Weight
412 KB
Volume
14
Category
Article
ISSN
1061-4036

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