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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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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Structural Analysis of Human Hemoglobin Variants by Molecular Secondary Ion Mass Spectrometry von Kazuo HIDAKA, 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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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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Abnormal pseudocholinesterase von 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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A new variant of butyrylcholinesterase gene detected in two patients in Yamaguchi Prefecture von Kazuo HIDAKA, Yoko WATANABE, Iwao IUCHI

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

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

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Amino Acid Substitution in Hemoglobin MAkita von SHIBATA, SUSUMU, MIYAJI, TAKAOKI, IUCHI, IWAO, OHBA, YUZO, YAMAMOTO, KIYOMI

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A SIMPLE METHOD FOR THE DETERMINATION OF HEMOGLOBIN A2 BY MEANS OF ISOELECTRIC FOCUSING ON POLYACRYLAMIDE GEL von Teruo HARANO, Satoshi UEDA, Iwao IUCHI, Susumu SHIBATA

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HB UBE-4 (α116 GLU→ALA): A SECOND INDEPENDENT INSTANCE OF A KOREAN FAMILY DISCOVERED BY HEMOGLOBIN SCREENINGS IN OKAYAMA DISTRICT von Kazuo HIDAKA, Iwao IUCHI, Satoshi UEDA, Susumu SHIBATA, Fumio HITOMI, Atsushi TAKESUE

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

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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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Hemoglobin Tochigi (β56-59 Deleted) A New Unstable Hemoglobin Discovered in a Japanese Family von SHIBATA, Susumu, MIYAJI, Takaoki, VEDA, Satoshi, MATSUOKA, Miyoko, IUCHI, Iwao, YAMADA, Kaneo, SHINKAI, Noboru

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