Subtelomere specific microarray based comparative genomic hybridisation: a rapid detection system for cryptic rearrangements in idiopathic mental retardation
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
Published in Journal of medical genetics (01.02.2004)
Published in Journal of medical genetics (01.02.2004)
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Mild form of beta-ketothiolase deficiency (mitochondrial acetoacetyl-CoA thiolase deficiency) in two Japanese siblings: identification of detectable residual activity and cross-reactive material in EB-transformed lymphocytes
Fukao, T, Kodama, A, Aoyanagi, N, Tsukino, R, Uemura, S, Song, X Q, Watanebe, H, Kuhara, T, Matsumoto, I, Orii, T, Kondo, N
Published in Clinical genetics (01.10.1996)
Published in Clinical genetics (01.10.1996)
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Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients
Hamabe, J, Fukushima, Y, Harada, N, Abe, K, Matsuo, N, Nagai, T, Yoshioka, A, Tonoki, H, Tsukino, R, Niikawa, N
Published in American journal of medical genetics (01.10.1991)
Published in American journal of medical genetics (01.10.1991)
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Ring chromosome 10: 46,XX,r(10)(p15→q26)
Tsukino, Ryuichi, Tsuda, Norihiko, Dezawa, Tohru, Ishii, Tadashi, Koike, Michio
Published in Journal of medical genetics (01.04.1980)
Published in Journal of medical genetics (01.04.1980)
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1p36 deletion syndrome with intestinal malrotation and annular pancreas
Minami, Koichi, Boshi, Haruna, Minami, Takaomi, Tamura, Akira, Yanagawa, Toshihiko, Uemura, Shigeru, Takifuji, Katsunari, Kurosawa, Kenji, Tsukino, Ryuichi, Izumi, Genkichi, Yoshikawa, Norishige
Published in European journal of pediatrics (01.03.2005)
Published in European journal of pediatrics (01.03.2005)
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Allelic variants of human calcitonin receptor in the Japanese population
NAKAMURA, M, ZHANG, Z.-Q, SHAN, L, HISA, T, SASAKI, M, TSUKINO, R, YOKOI, T, KANAME, A, KAKUDO, K
Published in Human genetics (1997)
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Published in Human genetics (1997)
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A case of congenital segmental absence of intestinal musculature
OHMORI, H., TSUKINO, R., KOIKE, M., KASHII, H.
Published in official journal of Congeital Anomalies Research Association of Japan (30.09.1983)
Published in official journal of Congeital Anomalies Research Association of Japan (30.09.1983)
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Successful arthroscopic treatment of pigmented villonodular synovitis of the knee in a patient with congenital deficiency of plasminogen activator inhibitor-1 and recurrent haemarthrosis
Matsui, H, Takahashi, Y, Matsunaga, T, Tanaka-Horie, T, Minowa, H, Sugimoto, M, Tsukino, R, Mii, Y, Giddings, J, Yoshioka, A
Published in Haemostasis (01.03.2001)
Published in Haemostasis (01.03.2001)
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Familial occurrence of oligomeganephronia
Kusuyama, Y, Tsukino, R, Oomori, H, Kuribayashi, K, Katayama, H, Koike, M, Saito, K
Published in Acta pathologica japonica (01.03.1985)
Published in Acta pathologica japonica (01.03.1985)
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Kabuki make-up (Niikawa-Kuroki) syndrome: a study of 62 patients
Niikawa, N, Kuroki, Y, Kajii, T, Matsuura, N, Ishikiriyama, S, Tonoki, H, Ishikawa, N, Yamada, Y, Fujita, M, Umemoto, H
Published in American journal of medical genetics (01.11.1988)
Published in American journal of medical genetics (01.11.1988)
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Recurrence Risk for the Second 21-Trisomic Children
FUJITA, Hiroko, HIRANO, Yasuko, SUGAWA, Tadashi, OGITA, Sachio, NOMOTO, Naoki, TSUKINO, Ryuichi
Published in Proceedings of the Japan Academy, Series B (1978)
Published in Proceedings of the Japan Academy, Series B (1978)
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Live varicella vaccine: prevention of nosocomial infection and protection of high risk infants from varicella infection
Sugino, H, Tsukino, R, Miyashiro, E, Dezawa, T, Shinohara, K, Uemura, S, Koike, M
Published in Biken journal (01.09.1984)
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Published in Biken journal (01.09.1984)
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