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Showing results 24 to 36 of 36 < previous

	Title	Author(s)	Issue Date
	Identification of two mutations (S50Y and 4173delC) in the CFTR gene from patients with congenital bilateral absence of vas deferens (CBAVD) Journal:Human Mutation	Zielenski, J Patrizio, P Markiewicz, D Asch, RH Tsui, LC	1997
	Increased prevalence of CFTR mutations and variants and decreased chloride secretion in primary sclerosing cholangitis Journal:Human Genetics	Sheth, S Shea, JC Bishop, MD Chopra, S Regan, MM Malmberg, E Walker, C Ricci, R Tsui, LC Durie, PR Zielenski, J Freedman, SD	2003
	Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families Journal:Human Genetics	Dork, T Neumann, T Wulbrand, U Wulf, B Kalin, N Maass, G Krawczak, M Guillermit, H Ferec, C Horn, G Klinger, K Kerem, BS Zielenski, J Tsui, LC Tummler, B	1992
	Modifier gene study of meconium ileus in cystic fibrosis: Statistical considerations and gene mapping results Journal:Human Genetics	Dorfman, R Li, W Sun, L Lin, F Wang, Y Sandford, A Paré, PD McKay, K Kayserova, H Piskackova, T MacEk, M Czerska, K Sands, D Tiddens, H Margarit, S Repetto, G Sontag, MK Accurso, FJ Blackman, S Cutting, GR Tsui, LC Corey, M Durie, P Zielenski, J Strug, LJ	2009
	Molecular genetics of cystic fibrosis Proceeding/Conference:Advances in Experimental Medicine and Biology	Tsui, LC Rommens, J Kerem, B Rozmahel, R Zielenski, J Kennedy, D Markiewicz, D Plavsic, N Chou, JL Bozon, D Dobbs, M	1991
	Mutations in the cystic fibrosis transmembrane regulator gene in patients with tropical calcific pancreatitis [8] Journal:American Journal of Gastroenterology	Bhatia, E Durie, P Zielenski, J Lam, D Sikora, SS Choudhuri, G Tsui, LC	2000
	Novel cystic fibrosis mutation (2215insG) two adolescent Taiwanese siblings Journal:Journal of the Formosan Medical Association	Wu, CL Shu, SG Zielenski, J Chiang, CD Tsui, LC	2000
	Screening for genetic mutations [1] Journal:Nature	Carlsson, C Jonsson, M Norden, B Dulay, MT Zare, RN Noolandi, J Nielsen, PE Tsui, LC Zielenski, J	1996
	Skipping of exon 12 as a consequence of a point mutation (1898+5G→T) in the cystic fibrosis transmembrane conductance regulator gene found in a consanguineous Chinese family Journal:Clinical Genetics	Zielenski, J Markiewicz, D Lin, SP Huang, FY YangFeng, TL Tsui, LC	1995
	Spectrum of CFTR mutations in Mexican cystic fibrosis patients: identification of five level mutations (W1098C, 846deIT, P750L, 4160insGGGC and 297-1G→A) Journal:Human Genetics	Orozco, L Velázquez, R Zielenski, J Tsui, LC Chávez, M Lezana, JL Saldana, Y Hernández, E Carnevale, A	2000
	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
	Two novel frameshift deletions (1924del7, 2055del9→A) in the CFTR gene in Mexican cystic fibrosis patients Journal:Human Mutation	Orozco, L Zielenski, J Markiewicz, D Villarreal, T Tsui, LC Lezana, JL Del Angel, RM	1997
	Uncertainty in the diagnosis of cystic fibrosis: Possible role of in vivo nasal potential difference measurements Journal:Journal of Pediatrics	Wilson, DC Ellis, L Zielenski, J Corey, M Ip, WF Tsui, LC Tullis, E Knowles, MR Durie, PR	1998

Showing results 24 to 36 of 36 < previous