Search Results - Mina, K.

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  1. 1
    Do aggregates of multiple questions better capture overall fish consumption than summary questions?

    Do aggregates of multiple questions better capture overall fish consumption than summary questions? by Mina, K., Fritschi, Lin, Knuiman, M.

    Published 2008
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  2. 2
    A Germline MTOR Mutation in Aboriginal Australian Siblings with Intellectual Disability, Dysmorphism, Macrocephaly, and Small Thoraces

    A Germline MTOR Mutation in Aboriginal Australian Siblings with Intellectual Disability, Dysmorphism, Macrocephaly, and Small Thoraces by Baynam, G., Overkov, A., Davis, M., Mina, K., Schofield, L., Allcock, R., Laing, N., Cook, M., Dawkins, Hugh, Goldblatt, J.

    Published 2015
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  3. 3
    An inverse association between preserved fish and prostate cancer: Results from a population-based case-control study in Canada

    An inverse association between preserved fish and prostate cancer: Results from a population-based case-control study in Canada by Mina, K., Fritschi, Lin, Johnson, K., Paulse, B., Dewar, R., Dryer, D., Kreiger, N., Kliewer, E., Robson, D., Fincham, S., Le, N.

    Published 2008
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  4. 4
    The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service.

    The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service. by Baynam, G., Pachter, N., McKenzie, F., Townshend, S., Slee, J., Kiraly-Borri, C., Vasudevan, A., Hawkins, A., Broley, S., Schofield, L., Verhoef, H., Walker, C., Molster, C., Blackwell, J., Jamieson, S., Tang, D., Lassmann, T., Mina, K., Beilby, J., Davis, M., Laing, N., Murphy, L., Weeramanthri, T., Dawkins, Hugh, Goldblatt, J.

    Published 2016
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  5. 5
    Genotype and phenotype spectrum of NRAS germline variants

    Genotype and phenotype spectrum of NRAS germline variants by Altmüller, F., Lissewski, C., Bertola, D., Flex, E., Stark, Z., Spranger, S., Baynam, Gareth, Buscarilli, M., Dyack, S., Gillis, J., Yntema, H., Pantaleoni, F., Van Loon, R., MacKay, S., Mina, K., Schanze, I., Tan, T., Walsh, M., White, S., Niewisch, M., García-Miñaúr, S., Plaza, D., Ahmadian, M., Cavé, H., Tartaglia, M., Zenker, M.

    Published 2017
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  6. 6
    Initiating an undiagnosed diseases program in the Western Australian public health system

    Initiating an undiagnosed diseases program in the Western Australian public health system by Baynam, G., Broley, S., Bauskis, A., Pachter, N., McKenzie, F., Townshend, S., Slee, J., Kiraly-Borri, C., Vasudevan, A., Hawkins, A., Schofield, L., Helmholz, Petra, Palmer, R., Kung, S., Walker, C., Molster, C., Lewis, B., Mina, K., Beilby, J., Pathak, G., Poulton, C., Groza, T., Zankl, A., Roscioli, T., Dinger, M., Mattick, J., Gahl, W., Groft, S., Tifft, C., Taruscio, D., Lasko, P., Kosaki, K., Wilhelm, H., Melegh, B., Carapetis, J., Jana, S., Chaney, G., Johns, A., Owen, P., Daly, F., Weeramanthri, T., Dawkins, H., Goldblatt, J.

    Published 2017
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  7. 7
    Improved diagnosis and care for rare diseases through implementation of precision public health framework

    Improved diagnosis and care for rare diseases through implementation of precision public health framework by Baynam, Gareth, Bowman, F., Lister, K., Walker, C., Pachter, N., Goldblatt, J., Boycott, K., Gahl, W., Kosaki, K., Adachi, T., Ishii, K., Mahede, T., McKenzie, Fiona, Townshend, S., Slee, J., Kiraly-Borri, C., Vasudevan, A., Hawkins, A., Broley, S., Schofield, L., Verhoef, H., Groza, T., Zankl, A., Robinson, P., Haendel, M., Brudno, M., Mattick, J., Dinger, M., Roscioli, T., Cowley, M., Olry, A., Hanauer, M., Alkuraya, F., Taruscio, D., Posada De La Paz, M., Lochmüller, H., Bushby, K., Thompson, R., Hedley, V., Lasko, P., Mina, K., Beilby, J., Tifft, C., Davis, M., Laing, N., Julkowska, D., Le Cam, Y., Terry, S., Kaufmann, P., Eerola, I., Norstedt, I., Rath, A., Suematsu, M., Groft, S., Austin, C., Draghia-Akli, R., Weeramanthri, Tarun, Molster, C., Dawkins, Hugh

    Published 2017
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