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Results: 1-9 |
Results: 9
High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness
Authors: Wiszniewski, W Sobieszczanska-Radoszewska, L Nowakowska-Szyrwinska, E Obersztyn, E Bal, J
Citation: W. Wiszniewski et al., High frequency of GJB2 gene mutations in Polish patients with prelingual nonsyndromic deafness, GENET TEST, 5(2), 2001, pp. 147-148
Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe
Authors: Dork, T Macek, M Mekus, F Tummler, B Tzountzouris, J Casals, T Krebsova, A Koudova, M Sakmaryova, I Macek, M 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, H 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
Citation: T. Dork et al., Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe, HUM GENET, 106(3), 2000, pp. 259-268
Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B
Authors: Wiszniewski, W Fondaneche, MC Lambert, N Masternak, K Picard, C Notarangelo, L Schwartz, K Bal, J Reith, W Alcaide, C de saint Basile, G Fischer, A Lisowska-Grospierre, B
Citation: W. Wiszniewski et al., Founder effect for a 26-bp deletion in the RFXANK gene in North African major histocompatibility complex class II-deficient patients belonging to complementation group B, IMMUNOGENET, 51(4-5), 2000, pp. 261-267
Managing the virtual team and controlling effectiveness
Authors: Bal, J Foster, P
Citation: J. Bal et P. Foster, Managing the virtual team and controlling effectiveness, INT J PROD, 38(17), 2000, pp. 4019-4032
Association between minihaplotypes and mutations at the PAH locus in polish hyperphenylalaninemic patients
Authors: Zekanowski, C Jurkowska, M Bal, J
Citation: C. Zekanowski et al., Association between minihaplotypes and mutations at the PAH locus in polish hyperphenylalaninemic patients, HUMAN HERED, 51(1-2), 2000, pp. 117-120
Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13
Authors: Zielenski, J Corey, M Rozmahel, R Markiewicz, D Aznarez, I Casals, T Larriba, S Mercier, B Cutting, GR Krebsova, A Macek, M Langfelder-Schwind, E Marshall, BC DeCelie-Germana, J Claustres, M Palacio, A Bal, J Nowakowska, A Ferec, C Estivill, X Durie, P Tsui, LC
Citation: J. Zielenski et al., Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13, NAT GENET, 22(2), 1999, pp. 128-129
Molecular characterization of Polish patients with classical galactosaemia
Authors: Zekanowski, C Radomyska, B Bal, J
Citation: C. Zekanowski et al., Molecular characterization of Polish patients with classical galactosaemia, J INH MET D, 22(5), 1999, pp. 679-A682
The efficacy of Nevirapine at low versus high viral loads
Authors: Russell, D Bal, J Anderson, J Moore, R Russell, J
Citation: D. Russell et al., The efficacy of Nevirapine at low versus high viral loads, SEVENTH EUROPEAN CONFERENCE ON CLINICAL ASPECTS AND TREATMENT OF HIV-INFECTION, 1999, pp. 119-123
Identification of mutations causing 6-pyruvoyl-tetrahydrobiopterin synthase deficiency in Polish patients with variant hyperphenylalaninemia
Authors: Zekanowski, C Nowacka, M Sendecka, E Slowik, M Cabalska, B Bal, J
Citation: C. Zekanowski et al., Identification of mutations causing 6-pyruvoyl-tetrahydrobiopterin synthase deficiency in Polish patients with variant hyperphenylalaninemia, MOL DIAGN, 3(4), 1998, pp. 237-239
Risultati: 1-9 |