CDKN1C ( p57 Kip2 ) Analysis in Beckwith – Wiedemann Syndrome ( BWS ) Patients : Genotype – Phenotype Correlations , Novel Mutations , and Polymorphisms

  • Romanelli V
  • Belinch A
  • Benito-sanz S
 et al. 
  • 2

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Authors

  • Valeria Romanelli

  • Alberta Belinch

  • Sara Benito-sanz

  • Victor Mart

  • Ricardo Gracia-bouthelier

  • Karen E Heath

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