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Author/Creator Kondoh, T

2. Lack of C20orf133 and FLRT3 mutations in 43 patients with Kabuki syndrome in Japan. Issue 7 (1st July 2008)

Authors:
Kuniba, H; Tsuda, M; Nakashima, M; Miura, S; Miyake, N; Kondoh, T; Matsumoto, T; Moriuchi, H; Ohashi, H; Kurosawa, K; Tonoki, H; Nagai, T; Okamoto, N; Kato, M; Fukushima, Y; Naritomi, K; Matsumoto, N; Kinoshita, A; Yoshiura, K-i; Niikawa, N
Journal:
Journal of medical genetics
Issue:
Volume 45:Issue 7(2008)
Page Start:
479
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

5. Sotos syndrome and haploinsufficiency of NSD1: clinical features of intragenic mutations and submicroscopic deletions. Issue 4 (1st April 2003)

Authors:
Nagai, T; Matsumoto, N; Kurotaki, N; Harada, N; Niikawa, N; Ogata, T; Imaizumi, K; Kurosawa, K; Kondoh, T; Ohashi, H; Tsukahara, M; Makita, Y; Sugimoto, T; Sonoda, T; Yokoyama, T; Uetake, K; Sakazume, S; Fukushima, Y; Naritomi, K
Journal:
Journal of medical genetics
Issue:
Volume 40:Issue 4(2003)
Page Start:
285
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

6. Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation. Issue 2 (2nd February 2004)

Authors:
Harada, N; Hatchwell, E; Okamoto, N; Tsukahara, M; Kurosawa, K; Kawame, H; Kondoh, T; Ohashi, H; Tsukino, R; Kondoh, Y; Shimokawa, O; Ida, T; Nagai, T; Fukushima, Y; Yoshiura, K; Niikawa, N; Matsumoto, N
Journal:
Journal of medical genetics
Issue:
Volume 41:Issue 2(2004)
Page Start:
130
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗