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CDKN1C
Genomic organization of the human p57KIP2 gene and its analysis in the G401 Wilms' tumor assay
Characterization of the human p57KIP2 gene: alternative splicing, insertion/deletion polymorphisms in VNTR sequences in the coding region, and mutational analysis
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome
Cancer Gene Census
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