يعرض 1 - 17 نتائج من 17 نتيجة بحث عن '"Tapscott, SJ"', وقت الاستعلام: 0.45s تنقيح النتائج
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    Academic Journal
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    Academic Journal
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    Academic Journal

    Relation: pii: ddn283; Knight, M. A., Hernandez, D., Diede, S. J., Dauwerse, H. G., Rafferty, I., van de Leemput, J., Forrest, S. M., Gardner, R. J. M., Storey, E., van Ommen, G. -J. B., Tapscott, S. J., Fischbeck, K. H. & Singleton, A. B. (2008). A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20. HUMAN MOLECULAR GENETICS, 17 (24), pp.3847-3853. https://doi.org/10.1093/hmg/ddn283.; http://hdl.handle.net/11343/303785

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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal
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    Academic Journal

    المساهمون: Sacconi, S, Lemmers, Rj, Balog, J, van der Vliet, Pj, Lahaut, P, van Nieuwenhuizen, Mp, Straasheijm, Kr, Debipersad, Rd, Vos Versteeg, M, Salviati, Leonardo, Casarin, A, Pegoraro, Elena, Tawil, R, Bakker, E, Tapscott, Sj, Desnuelle, C, van der Maarel, Sm

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/pmid/24075187; info:eu-repo/semantics/altIdentifier/wos/WOS:000326305600016; volume:93; issue:4; firstpage:744; lastpage:751; numberofpages:8; journal:AMERICAN JOURNAL OF HUMAN GENETICS; http://hdl.handle.net/11577/2682314; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-84885298881

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    Academic Journal

    المساهمون: Gonzalez, I, Ohsawa, N, Singer, Rh, Devillers, M, Ashizawa, T, Balasubramanyam, A, Cooper, Ta, Khajavi, M, LIA BALDINI, A, Miller, G, Philips, Av, Timchenko, Lt, Waring, J, Yamagata, H, Barbet, Jp, Klesert, Tr, Tapscott, Sj, Roses, Ad, Wagner, M, Baiget, M, Martorell, L, Browne, Gb, Eymard, B, Gourdon, G, Junien, C, Seznec, H, Carey, N, Gosling, M, Maire, P, Gennarelli, M, Sato, S, Ansved, T, Kvist, U, Eriksson, M, Furling, D, Chen, Ej, Housman, De, Luciano, B, Siciliano, M, Spring, N, Shimizu, M, Eddy, E, Morris, Ge, Krahe, R, Furuya, H, Adelman, J, Pribnow, D, Furutama, D, Mathieu, J, HILTON JONES, D, Kinoshita, M, Abbruzzese, C, Sinden, Rr, Wells, Rd, Pearson, Ce, Kobayashi, T, Johansson, A, Salvatori, Sergio, Perryman, B, Swanson, M, Gould, Fk, Harris, Se, Johnson, K, Mitchell, Am, Monckton, Dg, Winchester, Cl, Antonini, G, Day, Jw, Liquori, C, Ranum, Lpw, Westerlaken, J, Wieringa, B, Griffith, Jd, Michalowski, S, Moore, H, Hamshere, M, Korade, Z, Thornton, Ca, Jaeger, H, Lehmann, F, Moorman, Jr, Mounsey, Jp, Mahadevan, Ms

    Relation: info:eu-repo/semantics/altIdentifier/wos/WOS:000086109300004; volume:54; firstpage:1218; lastpage:1221; journal:NEUROLOGY; http://hdl.handle.net/11577/111540

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    Academic Journal

    المساهمون: Sancho S, Mongini T, Tanji K, Tapscott SJ, Walker WF, Weintraub H, Miller AD, Miranda AF

    وصف الملف: STAMPA

    Relation: info:eu-repo/semantics/altIdentifier/pmid/8361505; volume:329; issue:13; firstpage:915; lastpage:920; numberofpages:6; journal:NEW ENGLAND JOURNAL OF MEDICINE; http://hdl.handle.net/2318/133898

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    Academic Journal

    Relation: Timchenko, L., Tapscott, S., Cooper, T. and Monckton, D. (2002) Myotonic dystrophy: Discussion of molecular basis. Triple Repeat Diseases of the Nervous Systems , 516, pp. 27-45.

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    Academic Journal
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    Academic Journal