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New p57KIP2 mutations in Beckwith-Wiedemann syndrome.
Hatada I, Nabetani A, Morisaki H, Xin Z, Ohishi S, Tonoki H, Niikawa N, Inoue M, Komoto Y, Okada A, Steichen E, Ohashi H, Fukushima Y, Nakayama M, Mukai T. Hatada I, et al. Hum Genet. 1997 Oct;100(5-6):681-3. doi: 10.1007/s004390050573. Hum Genet. 1997. PMID: 9341892
An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome.
Hatada I, Ohashi H, Fukushima Y, Kaneko Y, Inoue M, Komoto Y, Okada A, Ohishi S, Nabetani A, Morisaki H, Nakayama M, Niikawa N, Mukai T. Hatada I, et al. Nat Genet. 1996 Oct;14(2):171-3. doi: 10.1038/ng1096-171. Nat Genet. 1996. PMID: 8841187
Genomic imprinting of human p57KIP2 and its reduced expression in Wilms' tumors.
Hatada I, Inazawa J, Abe T, Nakayama M, Kaneko Y, Jinno Y, Niikawa N, Ohashi H, Fukushima Y, Iida K, Yutani C, Takahashi S, Chiba Y, Ohishi S, Mukai T. Hatada I, et al. Hum Mol Genet. 1996 Jun;5(6):783-8. doi: 10.1093/hmg/5.6.783. Hum Mol Genet. 1996. PMID: 8776593
Allele-specific methylation and expression of an imprinted U2af1-rs1 (SP2) gene.
Hatada I, Kitagawa K, Yamaoka T, Wang X, Arai Y, Hashido K, Ohishi S, Masuda J, Ogata J, Mukai T. Hatada I, et al. Nucleic Acids Res. 1995 Jan 11;23(1):36-41. doi: 10.1093/nar/23.1.36. Nucleic Acids Res. 1995. PMID: 7870588 Free PMC article.
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