The hallmarks of CDKN1C (p57, KIP2) in cancer
Author:
Funder
Swedish Research Council, and the Swedish Cancer Society
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Oncology
Reference100 articles.
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4. Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith–Wiedemann syndrome (BWS) provides a novel genotype–phenotype correlation;Lam;J. Med. Genet.,1999
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