Authors: Kosho, T Nakamura, T Kaneko, T Tamura, M

Citation: T. Kosho et al., A case of neonatal-onset carbamoylphosphate synthase I deficiency treated by continuous haemodiafiltration, EUR J PED, 159(8), 2000, pp. 629-630

Authors: Ogata, T Wakui, K Kosho, T Muroya, K Yamanouchi, Y Takano, T Fukushima, Y Rappold, G Suzuki, Y

Citation: T. Ogata et al., Structural analysis of a rare rearranged Y chromosome and its bearing on genotype-phenotype correlation, AM J MED G, 92(4), 2000, pp. 256-259

Authors: Ogata, T Muroya, K Sasagawa, I Kosho, T Wakui, K Sakazume, S Ito, K Matsuo, N Ohashi, H Nagai, T

Citation: T. Ogata et al., Genetic evidence for a novel gene(s) involved in urogenital development on10q26, KIDNEY INT, 58(6), 2000, pp. 2281-2290

Authors: Ogata, T Kosho, T Wakui, K Fukushima, Y Yoshimoto, M Miharu, N

Citation: T. Ogata et al., Short stature homeobox-containing gene duplication on the der(X) chromosome in a female with 45,X/46,X, der(X), gonadal dysgenesis, and tall stature, J CLIN END, 85(8), 2000, pp. 2927-2930

Authors: Muroya, K Kosho, T Ogata, T Matsuo, M

Citation: K. Muroya et al., Female carriers of Xp22.3 deletion including MRX locus, AM J MED G, 84(4), 1999, pp. 384-385

Authors: Kosho, T Muroya, K Nagai, T Fujimoto, M Yokoya, S Sakamoto, H Hirano, T Terasaki, H Ohashi, H Nishimura, G Sato, S Matsuo, N Ogata, T

Citation: T. Kosho et al., Skeletal features and growth patterns in 14 patients with haploinsufficiency of SHOX: Implications for the development of Turner syndrome, J CLIN END, 84(12), 1999, pp. 4613-4621