Search Results - Oranwiroon, S.

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  1. 1
    Genotype and phenotype of haemophilia A in Thai patients

    Genotype and phenotype of haemophilia A in Thai patients by Yenchitsomanus, P., Akkarapatumwong, V., Pung-Amritt, P., Intorasoot, S., Thanootarakul, P., Oranwiroon, S., Veerakul, G., Mahasandana, C.

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  2. 2
    Mutations of the factor VIII gene in Thai hemophilia A patients

    Mutations of the factor VIII gene in Thai hemophilia A patients by Akkarapatumwong, V., Oranwiroon, S., Pung-amritt, P., Treesucon, A., Thanootarakul, P., Veerakul, G., Mahasandana, C., Panyim, S., Yenchitsomanus, P.

    Published in Human mutation
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  3. 3
    Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection

    Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection by Yenchitsomanus, P., Thanootarakul, P., Akkarapatumwong, V., Oranwiroon, S., Pung-Amritt, P., Veerakul, G., Mahasandana, C.

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  4. 4
    Determination of haemophilia A carrier status by mutation analysis

    Determination of haemophilia A carrier status by mutation analysis by Oranwiroon, S, Akkarapatumwong, V, Pung-Amritt, P, Treesucon, A, Veerakul, G, Mahasandana, C, Panyim, S, Yenchitsomanus, P

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  5. 5
    Frameshift mutations with severe and moderate clinical phenotypes in Thai hemophilia A patients

    Frameshift mutations with severe and moderate clinical phenotypes in Thai hemophilia A patients by Akkarapatumwong, Varaporn, Intorasoot, Sorasak, Oranwiroon, Sumalee, Thano-otarakul, Prapaporn, Pung-amritt, Parichat, Veerakul, Gavivann, Mahasandana, Chularatana, Panyim, Sakol, Yenchitsomanus, Pa-thai

    Published in Human mutation
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  6. 6
    Determination of haemophilia A carrier status by mutation analysis

    Determination of haemophilia A carrier status by mutation analysis by Oranwiroon, S., Akkarapatumwong, V., Pung-Amritt, P., Treesucon, A., Veerakul, G., Mahasandana, C., Panyim, S., Yenchitsomanus, P.

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  7. 7
    Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection

    Mutation causing exon 15 skipping and partial exon 16 deletion in factor VIII transcript, and a method for direct mutation detection by Yenchitsomanus, P, Thanootarakul, P, Akkarapatumwong, V, Oranwiroon, S, Pung-Amritt, P, Veerakul, G, Mahasandana, C

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