يعرض 1 - 10 نتائج من 1,026 نتيجة بحث عن '"Williams, SJ"', وقت الاستعلام: 1.58s تنقيح النتائج
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    المصدر: Scientific Reports, Vol 8, Iss 1, Pp 1-9 (2018)
    Rout, S P, Payne, L, Walker, S, Scott, T, Heard, P, Eccles, H, Bond, G, Shah, P, Bills, P, Jackson, B R, Boxall, S A, Laws, A P, Charles, C, Williams, S J & Humphreys, P N 2018, ' The Impact of Alkaliphilic Biofilm Formation on the Release and Retention of Carbon Isotopes from Nuclear Reactor Graphite ', Scientific Reports, vol. 8, 4455 . https://doi.org/10.1038/s41598-018-22833-5

    مصطلحات موضوعية: lcsh:R, lcsh:Medicine, lcsh:Q, lcsh:Science

    وصف الملف: application/pdf

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    المساهمون: Graduate School, Laboratory for General Clinical Chemistry, AGEM - Amsterdam Gastroenterology Endocrinology Metabolism, Laboratory Genetic Metabolic Diseases

    المصدر: The American journal of human genetics
    Ratbi, I, Falkenberg, K D, Sommen, M, Al-Sheqaih, N, Guaoua, S, Vandeweyer, G, Urquhart, J, Chandler, K E, Williams, S, Roberts, N, El Alloussi, M, Black, G, Ferdinandusse, S, Ramdi, H, Heimler, A, Fryer, A, Lynch, S-A, Cooper, N, Ong, K R, Smith, C E L, Inglehearn, C F, Mighell, A J, Elcock, C, Poulter, J A, Tischkowitz, M, Davies, S J, Sefiani, A, Mironov, A, Newman, W, Waterham, H R & Van Camp, G 2015, ' Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6. ', American Journal of Human Genetics, vol. 97, no. 4, pp. 535-545 . https://doi.org/10.1016/j.ajhg.2015.08.011
    American journal of human genetics, 97(4), 535-545. Cell Press

    وصف الملف: pdf; application/pdf