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つくばリポジトリ (Tulips-R) >
Browsing by Author "Okumura, Nobuo"
Showing results 1 to 3 of 3
| Issue Date | Title | Author(s) | | Aug-2010 | A C-terminal amino acid substitution in the γ-chain caused by a novel heterozygous frameshift mutation (Fibrinogen Matsumoto VII) results in hypofibrinogenaemia | Fujihara, Noriko; Haneishi, Ayumi; Yamauchi, Kazuyoshi; Terasawa, Fumiko; Ito, Toshiro; Ishida, Fumihiro; Okumura, Nobuo; 山内, 一由 |
| Sep-2010 | In vitro transcription of compound heterozygous hypofibrinogenemia Matsumoto IX; first identification of FGB IVS6 deletion of 4 nucleotides and FGG IVS3-2A > G causing abnormal RNA splicing | Terasawa, Fumiko; Kamijyo, Yuka; Fujihara, Noriko; Yamauchi, Kazuyoshi; Kumagai, Toshiko; Honda, Takayuki; Shigematsu, Satoshi; Okumura, Nobuo; 山内, 一由 |
| Jan-2011 | Quantitative monitoring of single nucleotide mutations by allele-specific quantitative PCR can be used for the assessment of minimal residual disease in patients with hematological malignancies throughout their clinical course | Taira, Chiaki; Matsuda, Kazuyuki; Kamijyo, Yuka; Sakashita, Kazuo; Ishida, Fumihiro; Kumagai, Toshiko; Yamauchi, Kazuyoshi; Okumura, Nobuo; Honda, Takayuki; 山内, 一由 |
Showing results 1 to 3 of 3
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