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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. Among authors: xin z. Hum Genet. 1997 Oct;100(5-6):681-3. doi: 10.1007/s004390050573. Hum Genet. 1997. PMID: 9341892
Sequence-based structural features between Kvlqt1 and Tapa1 on mouse chromosome 7F4/F5 corresponding to the Beckwith-Wiedemann syndrome region on human 11p15.5: long-stretches of unusually well conserved intronic sequences of kvlqt1 between mouse and human.
Yatsuki H, Watanabe H, Hattori M, Joh K, Soejima H, Komoda H, Xin Z, Zhu X, Higashimoto K, Nishimura M, Kuratomi S, Sasaki H, Sakaki Y, Mukai T. Yatsuki H, et al. Among authors: xin z. DNA Res. 2000 Jun 30;7(3):195-206. doi: 10.1093/dnares/7.3.195. DNA Res. 2000. PMID: 10907850
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