Analysis of germline CDKN1C (p57<sup>KIP2</sup>) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlation
Wayne Lam(Western General Hospital), Eamonn R. Maher(University of Birmingham), Wolf Reik(Altos Labs), Paul N. Schofield(Babraham Institute), Dian Donnai(St Mary's Hospital), Izuho Hatada(National Cerebral and Cardiovascular Center), Trevor Cole(Birmingham Women's Hospital), Johanna A. Joyce(University of Lausanne), Tsunehiro Mukai(Nishikyushu University), Sachiko Oh‐ishi(National Cerebral and Cardiovascular Center)
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