HKU Scholars Hub: Search

Search

Results 1-25 of 349 (Search time: 0.008 seconds).

previous
1
2
3
4
...
14
next

	Title	Author(s)	Issue Date
	Rapid nonradioactive detection of the major cystic fibrosis mutation Journal:American Journal of Human Genetics	Rommens, J Keram, BS Greer, W Chang, P Tsui, LC Ray, P	1990
	Cystic fibrosis mutations in North American populations of French ancestry: Analysis of Quebec French-Canadian and Louisiana Acadian families Journal:American Journal of Human Genetics	Rozen, R Schwartz, RH Hilman, BC Stanislovitis, P Horn, GT Klinger, K Daigneault, J De Braekleer, M Kerem, BS Tsui, LC Fujiwara, TM Morgan, K	1990
	The relation between genotype and phenotype in cystic fibrosis - Analysis of the most common mutation (ΔF 508) Journal:New England Journal of Medicine	Kerem, E Corey, M Kerem, BS Rommens, J Markiewicz, D Levison, H Tsui, LC Durie, P	1990
	Two patients with cystic fibrosis, nonsense mutations in each cystic fibrosis gene, and mild pulmonary disease Journal:New England Journal of Medicine	Cutting, GR Kasch, LM Rosenstein, BJ Tsui, LC Kazazian Jr, HH Antonarakis, SE	1990
	A cluster of highly polymorphic dinucleotide repeats in intron 17b of the cystic fibrosis transmembrane conductance regulator (CFTR) gene Journal:American Journal of Human Genetics	Zielenski, J Markiewicz, D Rininsland, F Rommens, J Tsui, LC	1991
	Genetic determination of exocrine pancreatic function in cystic fibrosis Journal:American Journal of Human Genetics	Kristidis, P Bozon, D Corey, M Markiewicz, D Rommens, J Tsui, LC Durie, P	1992
	Identification of the M1101K mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) gene and complete detection of cystic fibrosis mutations in the Hutterite population Journal:American Journal of Human Genetics	Zielenski, J Fujiwara, TM Markiewicz, D Paradis, AJ Anacleto, AI Richards, B Schwartz, RH Klinger, KW Tsui, LC Morgan, K	1993
	Fine mapping of the autosomal dominant split hand/split foot locus on chromosome 7, band q21.3-q22.1	Scherer, SW Poorkaj, P Allen, T Kim, J Geshuri, D Nunes, M Soder, S Stephens, K Pagon, RA Patton, MA Berg, MA Donlon, T Rivera, H Pfeiffer, RA Naritomi, K Hughes, H Genuardi, M Gurrieri, F Neri, G Lovrein, E Magenis, E Tsui, L-C Evans, JP	1994
	Evidence for locus heterogeneity in human autosomal dominant split hand/split foot malformation Journal:American Journal of Human Genetics	Palmer, SE Scherer, SW Kukolich, M Wijsman, EM Tsui, LC Stephens, K Evans, JP	1994
	CFTR gene variant for patients with congenital absence of vas deferens [3] Journal:American Journal of Human Genetics	Zielenski, J Patrizio, P Corey, M Handelin, B Markiewicz, D Asch, R Tsui, LC	1995
	Identification of a yeast artificial chromosome clone spanning a translocation breakpoint at 7q32.1 in a Smith-Lemli-Opitz syndrome patient Journal:American Journal of Human Genetics	Alley, TL Gray, BA Lee, SH Scherer, SW Tsui, LC Tint, GS Williams, CA Zori, R Wallace, MR	1995
	Hemizygous deletion of the syntaxin 1A gene in individuals with Williams syndrome: Letters to the editor	Osborne, LR Soder, S Shi, XM Pober, B Costa, T Scherer, SW Tsui, L-C	1997
	Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions Journal:Journal of General Physiology	Linsdell, P Tabcharani, JA Rommens, JM Hou, YX Chang, XB Tsui, LC Riordan, JR Hanrahan, JW	1997
	Lung disease in mice with cystic fibrosis Journal:Journal of Clinical Investigation	Kent, G Iles, R Bear, CE Huan, LJ Griesenbach, U McKerlie, C Frndova, H Ackerley, C Gosselin, D Radzioch, D O'Brodovich, H Tsui, LC Buchwald, M Tanswell, AK	1997
	Generation and chromosome mapping of expressed sequence tags (ESTs) from a human infant thymus Journal:Genome	Hwang, MY Kang, YJ Kim, YH Scherer, SW Tsui, LC Sohn, U	1999
	Involvement of the HLXB9 homeobox gene in Currarino syndrome [2] Journal:American Journal of Human Genetics	Belloni, E Martucciello, G Verderio, D Ponti, E Seri, M Jasonni, V Torre, M Ferrari, M Tsui, LC Scherer, SW	2000
	Transcriptional activation of immediate-early gene ETR101 by human T-cell leukaemia virus type I Tax Journal:Journal of General Virology	Chen, L Ma, S Li, B Fink, T Zachar, V Takahashi, M Cuttichia, J Tsui, LC Ebbesen, P Liu, X	2003
	The prevalence and clinical characteristics of cystic fibrosis in South Asian Canadian immigrants Journal:Archives of Disease in Childhood	MeiZahav, M Durie, P Zielenski, J Solomon, M Tullis, E Tsui, LC Corey, M	2005
	Cystic fibrosis: analysis of linkage of the disease locus to red cell and plasma protein markers Journal:Cytogenetics and Cell Genetics	Tsui, LC Cox, DW McAlpine, PJ Buchwald, M	1985
	Cystic fibrosis: Progress in mapping the disease locus using polymorphic DNA markers. I. Journal:Cytogenetics and Cell Genetics	Tsui, LC Zsiga, M Kennedy, D	1985
	Linkage of cystic fibrosis to the proα2(I) collagen gene, COL1A2, on chromosome 7	Buchwald, M Zsiga, M Markiewicz, D Plavsic, N Kennedy, D Zengerling, S Willard, HF Tsipouras, P Schmiegelow, K Schwartz, M Eiberg, H Mohr, J Barker, D Donis-Keller, H Tsui, LC	1986
	In situ hybridization of two cloned chromosome 7 sequences tightly linked to the cystic fibrosis locus Journal:Cytogenetics and Cell Genetics	Duncan, AMV Buchwald, M Tsui, LC	1988
	Localization of the human dihydrolipoamide dehydrogenase gene (DLD) to 7q31→q32 Journal:Cytogenetics and Cell Genetics	Scherer, SW Otulakowski, G Robinson, BH Tsui, LC	1991
	Refined localization of the asparagine synthetase gene (ASNS) to chromosome 7, region q21.3, and characterization of the somatic cell hybrid line 4AF/106/K015 Journal:Cytogenetics and Cell Genetics	Heng, HHQ Shi, XM Scherer, SW Andrulis, IL Tsui, LC	1994
	Assignment of the 5-hydroxytryptamine (serotonin) receptor 5A gene (HTR5A) to human chromosome band 7q36.1 Journal:Cytogenetics and Cell Genetics	Schanen, NC Scherer, SW Tsui, LC Francke, U	1996