Rapid detection of the 22q11.2 deletion with quantitative real-time PCR
Kariyazono, H., Ohno, T., Ihara, K., Igarashi, H., Joh-o, K., Ishikawa, S., Hara, T.
Published in Molecular and cellular probes (01.04.2001)
Published in Molecular and cellular probes (01.04.2001)
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Confirmation that the conotruncal anomaly face syndrome is associated with a deletion within 22q11.2
Matsuoka, R, Takao, A, Kimura, M, Imamura, S, Kondo, C, Joh-o, K, Ikeda, K, Nishibatake, M, Ando, M, Momma, K
Published in American journal of medical genetics (15.11.1994)
Published in American journal of medical genetics (15.11.1994)
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Thrombocytopenia in patients with 22q11.2 deletion syndrome and its association with glycoprotein Ib-beta
Kato, Taichi, Kosaka, Kazuki, Kimura, Misa, Imamura, Shin-Ichiro, Yamada, Osamu, Iwai, Kazumasa, Ando, Masahiko, Joh-o, Kunitaka, Kuroe, Kenji, Ohtake, Akira, Takao, Atsuyoshi, Momma, Kazuo, Matsuoka, Rumiko
Published in Genetics in medicine (01.03.2003)
Published in Genetics in medicine (01.03.2003)
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Molecular and clinical study of 183 patients with conotruncal anomaly face syndrome
MATSUOKA, R, KIMURA, M, OYAMA, K, SAJI, T, ANDO, M, TAKAO, A, MOMMA, K, SCAMBLER, P. J, MORROW, B. E, IMAMURA, S.-I, MINOSHIMA, S, SHIMIZU, N, YAMAGISHI, H, JOH-O, K, WATANABE, S
Published in Human genetics (01.07.1998)
Published in Human genetics (01.07.1998)
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Serum hepatocyte growth factor combined with vascular endothelial growth factor as a predictive indicator for the occurrence of coronary artery lesions in Kawasaki disease
OHNO, Takuro, YUGE, Tetsuji, KARIYAZONO, Hidehiko, IGARASHI, Hisaji, JOH-O, Kunitaka, KINUGAWA, Naoko, KUSUHARA, Kouichi, HARA, Toshiro
Published in European journal of pediatrics (01.02.2002)
Published in European journal of pediatrics (01.02.2002)
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Missense mutation of the beta-cardiac myosin heavy-chain gene in hypertrophic cardiomyopathy
Arai, S, Matsuoka, R, Hirayama, K, Sakurai, H, Tamura, M, Ozawa, T, Kimura, M, Imamura, S, Furutani, Y, Joh-o, K
Published in American journal of medical genetics (11.09.1995)
Published in American journal of medical genetics (11.09.1995)
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Molecular cytogenetic diagnosis of Williams syndrome
Hirota, H, Matsuoka, R, Kimura, M, Imamura, S, Joh-o, K, Ando, M, Takao, A, Momma, K
Published in American journal of medical genetics (23.08.1996)
Published in American journal of medical genetics (23.08.1996)
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