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Hiromasa Kobayashi

Department of Endocrinology

Kobe City General Hospital

4-6, Minatojimanakamachi

Hyogo

Japan

[email]@*.*.*.*.kobe.jp

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Affiliation

Department of Endocrinology, Kobe City General Hospital, 4-6, Minatojimanakamachi, Hyogo, Japan. 2002 - 2006

References

A novel heterozygous missense mutation in the vasopressin moiety is identified in a Japanese person with neurohypophyseal diabetes insipidus. Kobayashi, H., Fujisawa, I., Ikeda, K., Son, C., Iwakura, T., Yoshimoto, A., Kasahara, M., Ishihara, T., Ogawa, Y. J. Endocrinol. Invest. (2006) [Pubmed]
GC79/TRPS1 and tumorigenesis in humans. Kobayashi, H., Hino, M., Inoue, T., Nii, E., Ikeda, K., Son, C., Iwakura, T., Ishihara, T., Ogawa, Y. Am. J. Med. Genet. A (2005) [Pubmed]
Missense mutation of TRPS1 in a family of tricho-rhino-phalangeal syndrome type III. Kobayashi, H., Hino, M., Shimodahira, M., Iwakura, T., Ishihara, T., Ikekubo, K., Ogawa, Y., Nakao, K., Kurahachi, H. Am. J. Med. Genet. (2002) [Pubmed]