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	Title	Author(s)	Issue Date	Views
	CFTR mutation detection by multiplex heteroduplex (mHET) analysis on MDE gel. Journal:Methods in molecular medicine	Zielenski, J Aznarez, I Onay, T Tzounzouris, J Markiewicz, D Tsui, LC	2002	137
	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 Journal:Human Genetics	Dörk, T Macek Jr, M Mekus, F Tümmler, B Tzountzouris, J Casals, T Krebsová, A Koudová, M Sakmaryová, I Macek Sr, M Vávrová, V Zemková, D Ginter, E Petrova, NV Ivaschenko, T Baranov, V Witt, M Pogorzelski, A Bal, J Zékanowsky, 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 Kadási, L RavnikGlavač, M Glavač, D Komel, R Vouk, K Kučinskas, V Krumina, A Teder, M Kocheva, S Efremov, GD Onay, T Kirdar, B Malone, G Schwarz, M Zhou, Z Friedman, KJ Carles, S Claustres, M Bozon, D Verlingue, C Férec, C Tzetis, M Kanavakis, E Cuppens, H Bombieri, C Pignatti, PF Sangiuolo, F Jordanova, A Kusic, J Radojkovič, D Sertić, 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	2000	216
	Characterization of disease-associated mutations affecting an exonic splicing enhancer and two cryptic splice sites in exon 13 of the cystic fibrosis transmembrane conductance regulator gene Journal:Human Molecular Genetics	Aznarez, I Chan, EM Zielenski, J Blencowe, BJ Tsui, LC	2003	145
	Cystic fibrosis in Uruguay Journal:Genetics and Molecular Research	Luzardo, G Aznarez, I Crispino, B Mimbacas, A Martínez, L Poggio, R Zielenski, J Tsui, LC Cardoso, H	2002	113
	Detection of a cystic fibrosis modifier locus for meconium ileus on human chromosome 19q13 [3] Journal:Nature Genetics	Zielenski, J Corey, M Rozmahel, R Markiewicz, D Aznarez, I Casals, T Larriba, S Mercier, B Cutting, GR Krebsova, A Macek M, Jr Langfelder Schwind, E Marshall, BC DecelieGermana, J Claustres, M Palacio, A Bal, J Nowakowska, A Ferec, C Estivill, X Durie, P Tsui, LC	1999
	Exon skipping through the creation of a putative exonic splicing silencer as a consequence of the cystic fibrosis mutation R553X Journal:Journal of Medical Genetics	Aznarez, I Zielenski, J Rommens, JM Blencowe, BJ Tsui, LC	2007	193
	A systematic analysis of intronic sequences downstream of 5′ splice sites reveals a widespread role for U-rich motifs and TIA1/TIAL1 proteins in alternative splicing regulation Journal:Genome Research	Aznarez, I Barash, Y Shai, O He, D Zielenski, J Tsui, LC Parkinson, J Frey, BJ Rommens, JM Blencowe, BJ	2008	144

Showing results 2 to 8 of 8 < previous