Search Results - Kulseth, M.A.

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  1. 1
    Whole‐exome sequencing for diagnosis of hereditary ichthyosis

    Whole‐exome sequencing for diagnosis of hereditary ichthyosis by Sitek, J.C., Kulseth, M.A., Rypdal, K.B., Skodje, T., Sheng, Y., Retterstøl, L.

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    Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1

    Mutation analysis in Norwegian families with hereditary hemorrhagic telangiectasia: founder mutations in ACVRL1 by Heimdal, K., Dalhus, B., Rødningen, O.K., Kroken, M., Eiklid, K., Dheyauldeen, S., Røysland, T., Andersen, R., Kulseth, M.A.

    Published in Clinical genetics
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    A Highly Sensitive Chromogenic Microplate Assay for Quantification of Rat and Human Plasminogen

    A Highly Sensitive Chromogenic Microplate Assay for Quantification of Rat and Human Plasminogen by Kulseth, M.A., Helgeland, L.

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