Authors: Higashimoto, K Soejima, H Yatsuki, H Katsuki, T Mukai, T

Citation: K. Higashimoto et al., An NsiI RFLP in the human long QT intronic transcript 1 (LIT1), J HUM GENET, 45(2), 2000, pp. 96-97

Authors: Higashimoto, K Soejima, H Katsuki, T Mukai, T

Citation: K. Higashimoto et al., Identification of a novel single nucleotide polymorphism (SNP) in the human organic cation transporter-like 2-antisense (ORCTL2S) gene, J HUM GENET, 45(1), 2000, pp. 58-59

Authors: Yatsuki, H Watanabe, H Hattori, M Joh, K Soejima, H Komoda, H Xin, ZH Zhu, X Higashimoto, K Nishimura, M Kuratomi, S Sasaki, H Sakaki, Y Mukai, T

Citation: H. Yatsuki et al., 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, DNA RES, 7(3), 2000, pp. 195-206

Authors: Zhu, XK Higashimoto, K Soejima, H Yatsuki, H Sugihara, H Mukai, T Joh, K

Citation: Xk. Zhu et al., C11orf21, a novel gene within the Beckwith-Wiedemann syndrome region in human chromosome 11p15.5, GENE, 256(1-2), 2000, pp. 311-317

Authors: Xin, ZG Soejima, H Higashimoto, K Yatsuki, H Zhu, XK Satoh, Y Masaki, Z Kaneko, Y Jinno, Y Fukuzawa, R Hata, J Mukai, T

Citation: Zg. Xin et al., A novel imprinted gene, KCNQ1DN, within the WT2 critical region of human chromosome 11p15.5 and its reduced expression in Wilms' tumors, J BIOCHEM, 128(5), 2000, pp. 847-853