يعرض 1 - 10 نتائج من 174 نتيجة بحث عن '"Abdullah, U"', وقت الاستعلام: 1.31s تنقيح النتائج
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    دورية أكاديمية
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    دورية أكاديمية

    وصف الملف: application/pdf; application/zip

    العلاقة: https://openaccess.sgul.ac.uk/id/eprint/116030/1/awad257.pdfTest; https://openaccess.sgul.ac.uk/id/eprint/116030/6/awad257_supplementary_data.zipTest; Maroofian, R; Kaiyrzhanov, R; Cali, E; Zamani, M; Zaki, MS; Ferla, M; Tortora, D; Sadeghian, S; Saadi, SM; Abdullah, U; et al. Maroofian, R; Kaiyrzhanov, R; Cali, E; Zamani, M; Zaki, MS; Ferla, M; Tortora, D; Sadeghian, S; Saadi, SM; Abdullah, U; Karimiani, EG; Efthymiou, S; Yeşil, G; Alavi, S; Al Shamsi, AM; Tajsharghi, H; Abdel-Hamid, MS; Saadi, NW; Al Mutairi, F; Alabdi, L; Beetz, C; Ali, Z; Toosi, MB; Rudnik-Schöneborn, S; Babaei, M; Isohanni, P; Muhammad, J; Khan, S; Al Shalan, M; Hickey, SE; Marom, D; Elhanan, E; Kurian, MA; Marafi, D; Saberi, A; Hamid, M; Spaull, R; Meng, L; Lalani, S; Maqbool, S; Rahman, F; Seeger, J; Palculict, TB; Lau, T; Murphy, D; Mencacci, NE; Steindl, K; Begemann, A; Rauch, A; Akbas, S; Aslanger, AD; Salpietro, V; Yousaf, H; Ben-Shachar, S; Ejeskär, K; Al Aqeel, AI; High, FA; Armstrong-Javors, AE; Zahraei, SM; Seifi, T; Zeighami, J; Shariati, G; Sedaghat, A; Asl, SN; Shahrooei, M; Zifarelli, G; Burglen, L; Ravelli, C; Zschocke, J; Schatz, UA; Ghavideldarestani, M; Kamel, WA; Van Esch, H; Hackenberg, A; Taylor, JC; Al-Gazali, L; Bauer, P; Gleeson, JJ; Alkuraya, FS; Lupski, JR; Galehdari, H; Azizimalamiri, R; Chung, WK; Baig, SM; Houlden, H; Severino, M (2023) Biallelic MED27 variants lead to variable ponto-cerebello-lental degeneration with movement disorders. Brain, 146 (12). pp. 5031-5043. ISSN 1460-2156 https://doi.org/10.1093/brain/awad257Test SGUL Authors: Maroofian, Reza

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    دورية أكاديمية
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    دورية أكاديمية

    المساهمون: Engineering and Physical Sciences Research Council

    المصدر: Combustion Science and Technology ; page 1-23 ; ISSN 0010-2202 1563-521X

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    دورية أكاديمية

    العلاقة: pii: S2666-2477(22)00027-6; Asif, M., Kaygusuz, E., Shinawi, M., Nickelsen, A., Hsieh, T. -C., Wagle, P., Budde, B. S., Hochscherf, J., Abdullah, U., Höning, S., Nienberg, C., Lindenblatt, D., Noegel, A. A., Altmüller, J., Thiele, H., Motameny, S., Fleischer, N., Segal, I., Pais, L. ,. Hussain, M. S. (2022). De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway. HGG Adv, 3 (3), pp.100111-. https://doi.org/10.1016/j.xhgg.2022.100111Test.; http://hdl.handle.net/11343/310662Test

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    دورية أكاديمية
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    دورية أكاديمية

    وصف الملف: application/pdf; other

    العلاقة: http://edoc.mdc-berlin.de/21584/1/21584oa.pdfTest; http://edoc.mdc-berlin.de/21584/2/21584suppl.zipTest; De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway. Asif, M. and Kaygusuz, E. and Shinawi, M. and Nickelsen, A. and Hsieh, T.C. and Wagle, P. and Budde, B. and Hochscherf, J. and Abdullah, U. and Höning, S. and Nienberg, C. and Lindenblatt, D. and Noegel, A.A. and Altmüller, J. and Thiele, H. and Motameny, S. and Fleischer, N. and Segal, I. and Pais, L. and Tinschert, S. and Samra, N.G. and Savatt, J.M. and Rudy, N.L. and De Luca, C. and Fortugno, P. and White, S.M. and Krawitz, P. and Hurst, A.C.E. and Niefind, K. and Jose, J. and Brancati, F. and Nürnberg, P. and Hussain, M.S. Human Genetics and Genomics Advances 3 (3): 100111. 14 July 2022