يعرض 1 - 20 نتائج من 50 نتيجة بحث عن '"Wouter F.J. Feitz"', وقت الاستعلام: 0.55s تنقيح النتائج
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    المصدر: The American Journal of Human Genetics
    American Journal of Human Genetics, 104, 994-1006
    Kolvenbach, C M, Dworschak, G C, Frese, S, Japp, A S, Schuster, P, Wenzlitschke, N, Yilmaz, O, Lopes, F, Pryalukhin, A, Schierbaum, L, van der Zanden, L F M, Kause, F, Schneider, R, Taranta-Janusz, K, Szczepanska, M, Pawlaczyk, K, Newman, W G, Beaman, G M, Stuart, H M, Cervellione, R, Feitz, W F J, van Rooij, I A L M, Schreuder, M F, Steffens, M, Weber, S, Merz, W M, Feldkotter, M, Hoppe, B, Thiele, H, Altmuller, J, Berg, C, Kristiansen, G, Ludwig, M, Reutter, H, Woolf, A S, Hilderbrandt, F, Grote, P, Zaniew, M, Odermatt, B & Hilger, A C 2019, ' Rare Variants in BNC2 are implicated in autosomal dominant congenital lower urinary tract obstruction ', American Journal of Human Genetics . https://doi.org/10.1016/j.ajhg.2019.03.023
    American Journal of Human Genetics
    American Journal of Human Genetics, 104, 5, pp. 994-1006

    وصف الملف: application/pdf; application/octet-stream

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    المساهمون: von Lowtzow, C, Hofmann, A, Zhang, R, Marsch, F, Ebert, Ak, Rösch, W, Stein, R, Boemers, Tm, Hirsch, K, Marcelis, C, Feitz, Wf, Brusco, A, Migone, N, DI GRAZIA, Massimo, Moebus, S, Nöthen, Mm, Reutter, H, Ludwig, M, Draaken, M.

    المصدر: BMC Medical Genetics, 17, 1, pp. 35-35
    BMC Medical Genetics, 17, 35-35
    BMC Medical Genetics

    وصف الملف: ELETTRONICO; application/pdf

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    المصدر: Human Molecular Genetics
    Human Molecular Genetics, 23, 20, pp. 5536-44
    Human molecular genetics 23(20), 5536-5544 (2014). doi:10.1093/hmg/ddu259
    Human Molecular Genetics, 23, 5536-44
    Reutter, H, Draaken, M, Pennimpede, T, Wittler, L, Brockschmidt, F F, Ebert, A-K, Bartels, E, Rösch, W, Boemers, T M, Hirsch, K, Schmiedeke, E, Meesters, C, Becker, T, Stein, R, Utsch, B, Mangold, E, Nordenskjöld, A, Barker, G, Kockum, C C, Zwink, N, Holmdahl, G, Läckgren, G, Jenetzky, E, Feitz, W F, Marcelis, C, Wijers, C H W, van Rooij, I A L M, Gearhart, J P, Herrmann, B G, Ludwig, M, Boyadjiev, S A, Nöthen, M M & Mattheisen, M 2014, ' Genome-wide association study and mouse expression data identify a highly conserved 32kb intergenic region between WNT3 and WNT9b as possible susceptibility locus for isolated classic exstrophy of the bladder ', Human Molecular Genetics . https://doi.org/10.1093/hmg/ddu259

    وصف الملف: application/pdf

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    المصدر: Journal of Pediatric Urology, 8, 59-66
    Journal of Pediatric Urology, 8, 1, pp. 59-66

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    المساهمون: Urology, Paediatric Urology, Pediatric surgery, Human genetics, ICaR - Circulation and metabolism, Groningen Institute for Gastro Intestinal Genetics and Immunology (3GI)

    المصدر: PLoS ONE
    van Eerde, A M, Duran, K, van Riel, E, de Kovel, C G F, Koeleman, B P C, Knoers, N V A M, Renkema, K Y, van der Horst, H J R, Bokenkamp, A, van Hagen, J M, Van den Berg, L H, Wolffenbuttel, K P, van den Hoek, J, Feitz, W F, De Jong, T P V M, Giltay, J C & Wijmenga, C 2012, ' Genes in the Ureteric Budding Pathway: Association Study on Vesico-Ureteral Reflux Patients ', PLoS ONE, vol. 7, no. 4, e31327 . https://doi.org/10.1371/journal.pone.0031327
    PLoS ONE, 7(4). Public Library of Science
    PLoS ONE, 7(4):e31327. Public Library of Science
    PLoS One, 7
    PLoS ONE, Vol 7, Iss 4, p e31327 (2012)
    PLoS One, 7, 4
    PLoS One (print), 7(4). Public Library of Science
    PLoS ONE, 7(4):e31327. PUBLIC LIBRARY SCIENCE

    وصف الملف: application/pdf

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