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Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation
  1. Professor Maher.
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Citation

Lam WWK, Hatada I, Ohishi S, et al
Analysis of germline CDKN1C (p57KIP2) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation

Publication history

  • Received November 19, 1998
  • Revised March 8, 1999
  • First published July 1, 1999.
Online issue publication 
July 01, 1999

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