L A Larsen|M Christiansen|J Vuust|P S Andersen - JoVE Visualize

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Pharmacogenomics|November 28, 2001

Recent developments in high-throughput mutation screeningL A Larsen, M Christiansen, J Vuust, et al.

Human Mutation|April 29, 1999

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variantsL A Larsen, M Christiansen, J Vuust, et al.

Combinatorial Chemistry & High Throughput Screening|October 18, 2000

High throughput mutation screening by automated capillary electrophoresisL A Larsen, M Christiansen, J Vuust, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|March 25, 1999

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndromeL A Larsen, P S Andersen, J K Kanters, et al.

Scandinavian Cardiovascular Journal : SCJ|February 24, 2001

A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathyO Havndrup, H Bundgaard, P S Andersen, et al.

Journal of Cardiovascular Electrophysiology|July 8, 1998

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndromeJ K Kanters, L A Larsen, M Orholm, et al.

Human Mutation|October 23, 2001

Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresisL A Larsen, M Johnson, C Brown, et al.

European Journal of Human Genetics : EJHG|September 14, 1999

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 geneL A Larsen, I Fosdal, P S Andersen, et al.

Journal of Molecular and Cellular Cardiology|May 18, 1999

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chainH Bundgaard, O Havndrup, P S Andersen, et al.

Clinical Chemistry|July 27, 2001

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndromeL A Larsen, P S Andersen, J Kanters, et al.

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Showing results (1-10 of 437) with videos related to

Sort By:

Pageof 44

Pharmacogenomics|November 28, 2001

Recent developments in high-throughput mutation screeningL A Larsen, M Christiansen, J Vuust, et al.

Human Mutation|April 29, 1999

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: robust multiplex analysis and pattern-based identification of allelic variantsL A Larsen, M Christiansen, J Vuust, et al.

Combinatorial Chemistry & High Throughput Screening|October 18, 2000

High throughput mutation screening by automated capillary electrophoresisL A Larsen, M Christiansen, J Vuust, et al.

Clinica Chimica Acta; International Journal of Clinical Chemistry|March 25, 1999

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndromeL A Larsen, P S Andersen, J K Kanters, et al.

Scandinavian Cardiovascular Journal : SCJ|February 24, 2001

A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathyO Havndrup, H Bundgaard, P S Andersen, et al.

Journal of Cardiovascular Electrophysiology|July 8, 1998

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndromeJ K Kanters, L A Larsen, M Orholm, et al.

Human Mutation|October 23, 2001

Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresisL A Larsen, M Johnson, C Brown, et al.

European Journal of Human Genetics : EJHG|September 14, 1999

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 geneL A Larsen, I Fosdal, P S Andersen, et al.

Journal of Molecular and Cellular Cardiology|May 18, 1999

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chainH Bundgaard, O Havndrup, P S Andersen, et al.

Clinical Chemistry|July 27, 2001

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndromeL A Larsen, P S Andersen, J Kanters, et al.

Pageof 44