Structural Analysis of Human Hemoglobin Variants by Molecular Secondary Ion Mass Spectrometry von Kazuo HIDAKA, Iwao IUCHI

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Identification of missense mutation (G365R) of the butyrylcholinesterase (BCHE) gene in a Japanese patient with familial cholinesterasemia von Sakamoto, N, Maeda, T, Hidaka, K, Teranishi, T, Toyoda, M, Onishi, Y, Kuroda, S, Sakaguchi, K, Fujisawa, T, Maeda, M, Watanabe, Y, Iuchi, I

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The first instance of nonsense mutation (BChE, 400 stop) in exon 2 of the butyrylcholinesterase gene detected in Yamaguchi Prefecture von Kazuo HIDAKA, Toshiko YAMASAKI, Iwao IUCHI

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Some Clinical and Molecular Aspects of Hemoglobinopathy Detected by Our Screening Test for the Past 11 Years von Kazuo HIDAKA, Iwao IUCHI

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Another Japanese Kindred of Pseuocholinesterasemia von IUCHI, Iwao, SHIBATA, Susumu

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Identification of a Missense Mutation (LDH-H： R171P) in a Lactate Dehydrogenase Deficiency Patient Using the Reverse Transcription-Polymerase Chain Reaction von Kazuo HIDAKA, Mayumi HIGASHI, Yoko WATANABE, Naoki UEDA, Yohsuke MINATOGAWA, Iwao IUCHI

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Abnormal pseudocholinesterase von Iuchi, Iwao

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The First Instance of Hemoglobin E in a Japanese Family von SHIBATA, Susumu, IUCHI, Iwao, HAMILTON, Howard B.

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An improved diacetylmonoxime method for the determination of urea in blood and urine von Motoshi, Kitamura, Iwao, Iuchi

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EFFECT OF ERYTHROPOIETIN UPON HEMOGLOBIN BIOSYNTHESIS von Kraus, Lorraine M., Iuchi, Iwao, Kraus, Brother Thomas

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Hereditary Nigremia and Hemoglobin MIwate von SHIBATA, Susumu, TAMURA, Akira, IUCHI, Iwao, MIYAJI, Takaoki

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Secure parent node selection scheme in route construction to exclude attacking nodes from RPL network von Kenji, Iuchi, Matsunaga, Takumi, Toyoda, Kentaroh, Sasase, Iwao

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A new variant of butyrylcholinesterase gene detected in two patients in Yamaguchi Prefecture von Kazuo HIDAKA, Yoko WATANABE, Iwao IUCHI

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Gene analysis of genomic DNA from stored serum by polymerase chain reaction: identification of three missense mutations in patients with cholinesterasemia and ABO genotyping von Hidaka, Kazuo, Watanabe, Yoko, Tomita, Masafumi, Ueda, Naoki, Higashi, Mayumi, Minatogawa, Yohsuke, Iuchi, Iwao

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Identification of a point mutation associated with a silent phenotype of human serum butyrylcholinesterase – a case of familial cholinesterasemia von Sakamoto, Norikazu, Hidaka, Kazuo, Fujisawa, Takashi, Maeda, Mitsuo, Iuchi, Iwao

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Cystinuria (Types 1 and 3) Found in a Kindred of Silent-gene Pseudocholinesterasemia von IUCHI, Iwao, AMENO, Shigeko, MATSUO, Mitsuo, SHIBATA, Susumu

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Diversity of Human ?-Globin Gene Loci Including a Quadruplicated Arrangement von Shimasaki, Shunichi, Iuchi, Iwao

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Nonsense mutation in exon 2 of the butyrylcholinesterase gene: a case of familial cholinesterasemia von Hidaka, Kazuo, Iuchi, Iwao, Yamasaki, Toshiko, Ueda, Naoki, Hukano, Kouichi

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A Consanguineous Kindred of Serum Pseudocholinesterase Anomaly found in Japan von SHIBATA, Susumu, IUCHI, Iwao, HASHIMOTO, Yasuharu, SHODA, Takaaki

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First case of missense mutation (LDH-H:R171P) in exon 4 of the lactate dehydrogenase gene detected in a Japanese patient von Hidaka, K., Ueda, Naoki, Hirata, Ikuo, Watanabe, Yoko, Minatogawa, Yosuke, Iuchi, Iwao

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