يعرض 1 - 10 نتائج من 19 نتيجة بحث عن '"Sushree Sangita Sahoo"', وقت الاستعلام: 0.98s تنقيح النتائج
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    المصدر: Haematologica
    Pastor, V B, Sahoo, S, Boklan, J, Schwabe, G C, Saribeyoglu, E, Strahm, B, Lebrecht, D, Voss, M, Bryceson, Y T, Erlacher, M, Ehninger, G, Niewisch, M, Schlegelberger, B, Baumann, I, Achermann, J C, Shimamura, A, Hochrein, J, Tedgård, U, Nilsson, L, Hasle, H, Boerries, M, Busch, H, Niemeyer, C M & Wlodarski, M W 2018, ' Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7 ', Haematologica, vol. 103, no. 3, pp. 427-437 . https://doi.org/10.3324/haematol.2017.180778

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    المصدر: Frontiers in Immunology, Vol 8 (2017)
    Speckmann, Carsten; Sahoo, Sushree Sangita; Rizzi, Marta; Hirabayashi, Shinsuke; Karow, Axel; Serwas, Nina Kathrin; Hoemberg, Marc; Damatova, Natalja; Schindler, Detlev; Vannier, Jean-Baptiste; Boulton, Simon J; Pannicke, Ulrich; Göhring, Gudrun; Thomay, Kathrin; Verdu-Amoros, J J; Hauch, Holger; Woessmann, Wilhelm; Escherich, Gabriele; Laack, Eckart; Rindle, Liliana; ... (2017). Clinical and Molecular Heterogeneity of RTEL1 Deficiency. Frontiers in immunology, 8(449), p. 449. Frontiers Research Foundation 10.3389/fimmu.2017.00449 <http://dx.doi.org/10.3389/fimmu.2017.00449>
    Frontiers in Immunology

    وصف الملف: application/pdf

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    المصدر: PLoS ONE, Vol 7, Iss 12, p e52043 (2012)
    PLoS ONE

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