Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors (Q35249129)
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(P577) Friday, August 1, 1997
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(P1476) "Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors" (language: en)
(P2093) D O'Keefe
D Dao
L Zhao
R Sanderson
D Warburton
L Weiss
B Tycko
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