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Kimura, Y
Muroya, K
Hiramatsu, H
Naito, T
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Authors:
Muroya, K
Kinoshita, E
Kamimaki, T
Matsuo, N
Yorifugi, T
Ogata, T
Citation: K. Muroya et al., Deletion mapping and X inactivation analysis of a non-specific mental retardation gene at Xp21.3-Xp22.11, J MED GENET, 36(3), 1999, pp. 187-191
Authors:
Kosho, T
Muroya, K
Nagai, T
Fujimoto, M
Yokoya, S
Sakamoto, H
Hirano, T
Terasaki, H
Ohashi, H
Nishimura, G
Sato, S
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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
Authors:
Yamada, S
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Nishigori, H
Sho, K
Mabe, H
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Moriya, N
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Ogata, T
Onigata, K
Morikawa, A
Inoue, I
Takeda, J
Citation: S. Yamada et al., Identification of mutations in the hepatocyte nuclear factor-1 alpha gene in Japanese subjects with early-onset NIDDM and functional analysis of the mutant proteins, DIABETES, 48(3), 1999, pp. 645-648