An imprinted gene p57KIP2 is mutated in Beckwith–Wiedemann syndromeIzuho Hatada, Tsunehiro Mukai, Hirofumi Ohashi 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
Restriction landmark genomic scanning method and its various applicationsYoshihide Hayashizaki, Tsunehiro Mukai, Shinji Hirotsune et al.|Electrophoresis|1993Cited by 159
Mouse <i>U2af1</i> - <i>rs1</i> Is a Neomorphic Imprinted GeneAkira Nabetani, Tsunehiro Mukai, Izuho Hatada et al.|Molecular and Cellular Biology|1997Cited by 98
Domain Regulation of Imprinting Cluster in Kip2/Lit1 Subdomain on Mouse Chromosome 7F4/F5: Large-Scale DNA Methylation Analysis Reveals That DMR-Lit1 Is a Putative Imprinting Control RegionHitomi Yatsuki, Tsunehiro Mukai, Keiichiro Joh et al.|Genome Research|2002Cited by 67