検索結果 - Rhodes, D A

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

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Magnetism in semiconducting molybdenum dichalcogenides 著者: 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.

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