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(Aston University), Wolf Reik(F5 Networks (United States)), Paul N. Schofield(Babraham Institute), Dian Donnai(Manchester University NHS Foundation Trust), Izuho Hatada(National Cerebral and Cardiovascular Center), Trevor Cole(Birmingham Women's Hospital), Johanna A. Joyce(University Hospital of Lausanne), Tsunehiro Mukai(National Cerebral and Cardiovascular Center), Sachiko Oh‐ishi(National Cerebral and Cardiovascular Center)
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