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L A Larsen

Showing results (11-20 of 39) with videos related to

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European Journal of Human Genetics : EJHG|September 26, 2001
Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with AsiaL A Larsen, J Vuust, M Nystad, et al.
Human Genetics|October 28, 1997
High-throughput analysis of fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresisL A Larsen, K Grønskov, B Nørgaard-Pedersen, et al.
Clinical Genetics|November 24, 1999
Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 geneP S Andersen, O Havndrup, H Bundgaard, et al.
The American Journal of Cardiology|May 30, 2001
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young ageO Havndrup, H Bundgaard, P S Andersen, 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.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 10, 2013
Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twinsP S Andersen, L A Larsen, V G Fowler, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|April 25, 2016
Editor's Choice - High Heritability of Liability to Abdominal Aortic Aneurysms: A Population Based Twin StudyT M M Joergensen, K Christensen, J S Lindholt, 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.
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.
Pageof 4

Showing results (11-20 of 39) with videos related to

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Pageof 4
European Journal of Human Genetics : EJHG|September 26, 2001
Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with AsiaL A Larsen, J Vuust, M Nystad, et al.
Human Genetics|October 28, 1997
High-throughput analysis of fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresisL A Larsen, K Grønskov, B Nørgaard-Pedersen, et al.
Clinical Genetics|November 24, 1999
Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 geneP S Andersen, O Havndrup, H Bundgaard, et al.
The American Journal of Cardiology|May 30, 2001
The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young ageO Havndrup, H Bundgaard, P S Andersen, 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.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 10, 2013
Risk factors for Staphylococcus aureus nasal colonization in Danish middle-aged and elderly twinsP S Andersen, L A Larsen, V G Fowler, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|April 25, 2016
Editor's Choice - High Heritability of Liability to Abdominal Aortic Aneurysms: A Population Based Twin StudyT M M Joergensen, K Christensen, J S Lindholt, 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.
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.
Pageof 4