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European Journal of Human Genetics : EJHG|January 1, 1995
A quality control study of CFTR mutation screening in 40 different European laboratories. The European Concerted Action on Cystic FibrosisH Cuppens, J J CassimanAmerican Journal of Respiratory and Critical Care Medicine|May 6, 1999
Genotype-phenotype correlations for the paranasal sinuses in cystic fibrosisM B Jorissen, K De Boeck, H CuppensJournal of Pharmaceutical and Biomedical Analysis|January 1, 1989
Identification of polysaccharides in pharmaceuticals by capillary gas chromatographyG Vanlaeke, H Cuppens, L Leyssens, et al.DNA and Cell Biology|July 1, 1990
Rapid detection of hypervariable regions by the polymerase chain reaction techniqueR Decorte, H Cuppens, P Marynen, et al.Genomics|December 1, 1993
Detection of 98.5% of the mutations in 200 Belgian cystic fibrosis alleles by reverse dot-blot and sequencing of the complete coding region and exon/intron junctions of the CFTR geneH Cuppens, P Marynen, C De Boeck, et al.Molecular and Cellular Probes|February 1, 1992
Simultaneous screening for 11 mutations in the cystic fibrosis transmembrane conductance regulator gene by multiplex amplification and reverse dot-blotH Cuppens, I Buyse, M Baens, et al.Human Mutation|March 3, 1998
Detection of five novel mutations of the cystic fibrosis transmembrane regulator (CFTR) gene in Pakistani patients with cystic fibrosis: Y569D, Q98X, 296+12(T>C), 1161delC and 621+2(T>C)G Malone, A Haworth, M J Schwarz, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|January 21, 2014
The relative frequency of CFTR mutation classes in European patients with cystic fibrosisK De Boeck, A Zolin, H Cuppens, et al.FEBS Letters|May 17, 2000
Suppressive interactions between mutations located in the two nucleotide binding domains of CFTRL Wei, A Vankeerberghen, M Jaspers, et al.Human Molecular Genetics|April 1, 1994
CFTR haplotype backgrounds on normal and mutant CFTR genesH Cuppens, H Teng, P Raeymaekers, et al.Pageof 5