المؤلفون: Metzger, S, Bauer, P, Tomiuk, J, Laccone, F, DiDonato, S, Gellera, C, Lange, H.W, Weirich-Schwaiger, H, Melegh, B, Havasi, V, Baliko, L, Epplen, J.T, Zaremba, J, Sulek, A, Basak, A.N, Soydan, E, Zidovska, J, Kebrdlova, V, Pandolfo, M, Ribai, P, Kadasi, L, Kvasnicova, M, Weber, B.H.F, Kreuz, F, Dose, M, Stuhrmann, M, Riess, O

المصدر: Aktuelle Neurologie ; volume 32, issue S 4 ; ISSN 0302-4350 1438-9428

الإتاحة: https://doi.org/10.1055/s-2005-919317Test

المؤلفون: Rautenstrauss, B, Nelis, E, Zerres, K, Parman, Y, Hahn, A, Muller-Felber, W, Rizzuto, N, Fabrizi, GM, Stuhrmann, M, Rudnik-Schoneborn, S, Zuchner, S, Schroder, JM, Buchheim, E, Straub, V, Klepper, JR, Huehne, K, Buttner, R, Senderek, J, Bergmann, C, Stendel, C, Kirfel, J, Verpoorten, N, De Jonghe, P, Timmerman, V, Chrast, R, Verheijen, MHG, Lemke, G, Battaloglu, E, Erdem, S, Tan, E, Topaloglu, H

المساهمون: 169889

مصطلحات موضوعية: GENETİK VE HAYAT, Dahili Tıp Bilimleri, Tıbbi Genetik, Yaşam Bilimleri, Moleküler Biyoloji ve Genetik, Temel Bilimler, Sağlık Bilimleri, Yaşam Bilimleri (LIFE), Tıp

العلاقة: AMERICAN JOURNAL OF HUMAN GENETICS; Senderek J., Bergmann C., Stendel C., Kirfel J., Verpoorten N., De Jonghe P., Timmerman V., Chrast R., Verheijen M., Lemke G., et al., "Mutations in a gene encoding a novel SH3/TPR domain protein cause autosomal recessive Charcot-Marie-Tooth type 4C neuropathy", AMERICAN JOURNAL OF HUMAN GENETICS, cilt.73, ss.1106-1119, 2003; vv_1032021; av_c61aa37c-8792-4e7a-a9b5-8e09525a4c80; http://hdl.handle.net/20.500.12627/131348Test; https://doi.org/10.1086/379525Test; 73; 1106; 1119

الإتاحة: https://doi.org/20.500.12627/131348Test
https://doi.org/10.1086/379525Test
https://hdl.handle.net/20.500.12627/131348Test

المؤلفون: T�mmler, B., Stuhrmann, M.

المصدر: Der Internist ; volume 44, issue 0, page S7-S15 ; ISSN 0020-9554 1432-1289

مصطلحات موضوعية: Internal Medicine

الإتاحة: https://doi.org/10.1007/s00108-003-0965-xTest

المؤلفون: Groman, JD Hefferon, TW Casals, T Bassas, LS Estivill, X and Des Georges, M Guittard, C Koudova, M Fallin, MD and Nemeth, K Fekete, G Kadasi, L Friedman, K Schwarz, M and Bombieri, C Pignatti, PF Kanavakis, E Tzetis, M and Schwartz, M Novelli, G D'Apice, MR Sobczynska-Tomaszewska, A and Bal, J Stuhrmann, M Macek, M Claustres, M Cutting, GR

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______2127::d5e4b0bdf574645fb907eb132dff93f8Test
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3084818Test

المؤلفون: Stuhrmann, M., Spangenberg, A., Böhm, I., Reis, A., Schmidtke, J.

المصدر: PCR Topics ; page 89-91 ; ISBN 9783540529347 9783642759246

الإتاحة: https://doi.org/10.1007/978-3-642-75924-6_18Test

المؤلفون: Macek, M., Vavrova, V., Boehm, I., Stuhrmann, M., Reis, A., Duspisova, R., Jelinkova, E., Sperling, K., Krawczak, M., Schmidtke, J.

المصدر: Advances in Experimental Medicine and Biology ; The Identification of the CF (Cystic Fibrosis) Gene ; page 373-375 ; ISSN 0065-2598 2214-8019 ; ISBN 9781468459364 9781468459340

الإتاحة: https://doi.org/10.1007/978-1-4684-5934-0_42Test

المؤلفون: Heller, D., Schneider, U., Seifert, J., Cimander, K. F., Stuhrmann, M.

المصدر: Addiction Biology ; volume 6, issue 2, page 183-187 ; ISSN 1355-6215 1369-1600

الإتاحة: https://doi.org/10.1080/13556210020040271Test

المؤلفون: Stuhrmann, M, Bashawri, L., Ahmed, M. A., Al‐Awamy, B. H., Kühnau, W., Schmidtke, J., El‐Harith, E. A.

المصدر: British Journal of Haematology ; volume 112, issue 3, page 616-620 ; ISSN 0007-1048 1365-2141

الإتاحة: https://doi.org/10.1046/j.1365-2141.2001.02565.xTest

المؤلفون: OCKENGA, J, STUHRMANN, M, MANNS, M P

المصدر: Gut ; volume 49, issue 2, page 312.2-313 ; ISSN 0017-5749 1468-3288

مصطلحات موضوعية: Gastroenterology

الإتاحة: https://doi.org/10.1136/gut.49.2.312-aTest

المؤلفون: Dork, T, Macek, M, Mekus, F, Tummler, B, Tzountzouris, J, Casals, T, Krebsova, A, Koudova, M, Sakmaryova, I, Vavrova, V, Zemkova, D, Ginter, E, Petrova, NV, Ivaschenko, T, Baranov, V, Witt, M, Pogorzelski, A, Bal, J, Zekanowsky, C, Wagner, K, Stuhrmann, M, Bauer, I, Seydewitz, HH, Neumann, T, Jakubiczka, S, Kraus, C, Thamm, B, Nechiporenko, M, Livshits, L, Mosse, N, Tsukerman, G, Kadasi, L, Ravnik-Glavac, M, Glavac, D, Komel, R, Vouk, K, Kucinskas, V, Krumina, A, Teder, M, Kocheva, S, Efremov, GD, Onay, T, Kirdar, B, Malone, G, Schwarz, M, Zhou, ZQ, Friedman, KJ, Carles, S, Claustres, M, Bozon, D, Verlingue, C, Ferec, C, Tzetis, M, Kanavakis, E, Cuppens, Harry, Bombieri, C, Pignatti, PF, Sangiuolo, F, Jordanova, A, Kusic, J, Radojkovic, D, Sertic, J, Richter, D, Rukavina, AS, Bjorck, E, Strandvik, B, Cardoso, H, Montgomery, M, Nakielna, B, Hughes, D, Estivill, X, Aznarez, I, Tullis, E, Tsui, LC, Zielenski, J

مصطلحات موضوعية: transmembrane conductance regulator, identification, alleles, dna, recombination, heterogeneity, population, 90-percent, sequence, absence

العلاقة: Human Genetics vol:106 issue:3 pages:259-268; https://lirias.kuleuven.be/handle/123456789/159685Test

الإتاحة: https://lirias.kuleuven.be/handle/123456789/159685Test