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W E Highsmith

Showing results (21-30 of 35) with videos related to

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Genome Biology|December 12, 2001
Sources of nonlinearity in cDNA microarray expression measurementsL Ramdas, K R Coombes, K Baggerly, et al.
Clinical Genetics|June 15, 2005
A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chloridesW E Highsmith, K J Friedman, L H Burch, et al.
Electrophoresis|June 25, 1999
Use of DNA toolbox for the characterization of mutation scanning methods. II: evaluation of single-strand conformation polymorphism analysisW E Highsmith, A J Nataraj, Q Jin, et al.
Gut|October 18, 2005
Cystic fibrosis transmembrane regulator gene carrier status is a risk factor for young onset pancreatic adenocarcinomaR McWilliams, W E Highsmith, K G Rabe, et al.
Human Mutation|January 1, 1995
Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testingT W Prior, G D Wenger, A C Papp, et al.
Clinical Chemistry|December 1, 1990
Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotidesT W Prior, A C Papp, P J Snyder, et al.
Electrophoresis|June 25, 1999
Use of a DNA toolbox for the characterization of mutation scanning methods. I: construction of the toolbox and evaluation of heteroduplex analysisW E Highsmith, Q Jin, A J Nataraj, et al.
Annals of Internal Medicine|November 15, 1989
Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotypeA McConkie-Rosell, Y T Chen, D Harris, et al.
American Journal of Respiratory and Critical Care Medicine|October 1, 1995
Screening Young syndrome patients for CFTR mutationsK J Friedman, H Teichtahl, D M De Kretser, et al.
The New England Journal of Medicine|October 13, 1994
A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrationsW E Highsmith, L H Burch, Z Zhou, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Genome Biology|December 12, 2001
Sources of nonlinearity in cDNA microarray expression measurementsL Ramdas, K R Coombes, K Baggerly, et al.
Clinical Genetics|June 15, 2005
A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chloridesW E Highsmith, K J Friedman, L H Burch, et al.
Electrophoresis|June 25, 1999
Use of DNA toolbox for the characterization of mutation scanning methods. II: evaluation of single-strand conformation polymorphism analysisW E Highsmith, A J Nataraj, Q Jin, et al.
Gut|October 18, 2005
Cystic fibrosis transmembrane regulator gene carrier status is a risk factor for young onset pancreatic adenocarcinomaR McWilliams, W E Highsmith, K G Rabe, et al.
Human Mutation|January 1, 1995
Rapid DNA haplotyping using a multiplex heteroduplex approach: application to Duchenne muscular dystrophy carrier testingT W Prior, G D Wenger, A C Papp, et al.
Clinical Chemistry|December 1, 1990
Determination of carrier status in Duchenne and Becker muscular dystrophies by quantitative polymerase chain reaction and allele-specific oligonucleotidesT W Prior, A C Papp, P J Snyder, et al.
Electrophoresis|June 25, 1999
Use of a DNA toolbox for the characterization of mutation scanning methods. I: construction of the toolbox and evaluation of heteroduplex analysisW E Highsmith, Q Jin, A J Nataraj, et al.
Annals of Internal Medicine|November 15, 1989
Mild cystic fibrosis linked to chromosome 7q22 markers with an uncommon haplotypeA McConkie-Rosell, Y T Chen, D Harris, et al.
American Journal of Respiratory and Critical Care Medicine|October 1, 1995
Screening Young syndrome patients for CFTR mutationsK J Friedman, H Teichtahl, D M De Kretser, et al.
The New England Journal of Medicine|October 13, 1994
A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrationsW E Highsmith, L H Burch, Z Zhou, et al.
Pageof 4