An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndromeIzuho Hatada, Tsunehiro Mukai, Akira Okada et al.|Nature Genetics|1996Cited by 385
Analysis of germline CDKN1C (p57<sup>KIP2</sup>) mutations in familial and sporadic Beckwith-Wiedemann syndrome (BWS) provides a novel genotype-phenotype correlationWayne Lam, Eamonn R. Maher, Izuho Hatada et al.|Journal of Medical Genetics|1999Cited by 178
Allele-specific methylation and expression of an imprinted U2afl-rsl (SP2) geneIzuho Hatada, Tsunehiro Mukai, Jun Ogata et al.|Nucleic Acids Research|1995Cited by 53