Rezultati - Rhodes, D A

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  1. 1
    Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis.

    Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis. od Rhodes, D A, Raha-Chowdhury, R, Cox, T M, Trowsdale, J

    Izdano 1997
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  2. 2
    Magnetism in semiconducting molybdenum dichalcogenides

    Magnetism in semiconducting molybdenum dichalcogenides od Guguchia, Z., Kerelsky, A., Edelberg, D., Banerjee, S., von Rohr, F., Scullion, D., Augustin, M., Scully, M., Rhodes, D. A., Shermadini, Z., Luetkens, H., Shengelaya, A., Baines, C., Morenzoni, E., Amato, A., Hone, J. C., Khasanov, R., Billinge, S. J. L., Santos, E., Pasupathy, A. N., Uemura, Y. J.

    Izdano 2018
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