Idiopathic hypoparathyroidism in two patients with 22q11 microdeletion.

Por Makita, Y, Masuno, M, Maizumi, K, Tachibana, K, Kuroki, Y, Kurahashi, H
Publicado em 1995

The constitutional t(11;22): implications for a novel mechanism responsible for gross chromosomal rearrangements

Por Kurahashi, H, Inagaki, H, Ohye, T, Kogo, H, Tsutsumi, M, Kato, T, Tong, M, Emanuel, BS
Publicado em 2010

Deletion mapping of 22q11 in CATCH22 syndrome: identification of a second critical region.

Por Kurahashi, H., Nakayama, T., Osugi, Y., Tsuda, E., Masuno, M., Imaizumi, K., Kamiya, T., Sano, T., Okada, S., Nishisho, I.
Publicado em 1996

Age-related changes in surface antigens on peripheral lymphocytes of healthy children.

Por Osugi, Y, Hara, J, Kurahashi, H, Sakata, N, Inoue, M, Yumura-Yagi, K, Kawa-Ha, K, Okada, S, Tawa, A
Publicado em 1995

A kerato-epithelin (betaig-h3) mutation in lattice corneal dystrophy type IIIA.

Por Yamamoto, S, Okada, M, Tsujikawa, M, Shimomura, Y, Nishida, K, Inoue, Y, Watanabe, H, Maeda, N, Kurahashi, H, Kinoshita, S, Nakamura, Y, Tano, Y
Publicado em 1998

Microdeletion 22q11.2: clinical data and deletion size

Por KERSTJENS-FREDERI..., W, KURAHASHI, H, DRISCOLL, D, BUDARF, M, EMANUEL, B, BEATTY, B, SCHEIDL, T, SIEGEL-BARTELT, J, HENDERSON, K, CYTRYNBAUM, C, NIE, G, TESHIMA, I
Publicado em 1999

Homozygosity mapping of a gene responsible for gelatinous drop-like corneal dystrophy to chromosome 1p.

Por Tsujikawa, M, Kurahashi, H, Tanaka, T, Okada, M, Yamamoto, S, Maeda, N, Watanabe, H, Inoue, Y, Kiridoshi, A, Matsumoto, K, Ohashi, Y, Kinoshita, S, Shimomura, Y, Nakamura, Y, Tano, Y
Publicado em 1998