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L A Larsen

Showing results (21-30 of 39) with videos related to

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Pharmaceutical Research|April 17, 2001
Hepatic disposition of fexofenadine: influence of the transport inhibitors erythromycin and dibromosulphothaleinR W Milne, L A Larsen, K L Jørgensen, 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.
The American Journal of Clinical Nutrition|July 1, 1991
Report on the Fourth Conference for Federally Supported Human Nutrition Research Units and CentersD E Danford, V S Hubbard, G F Combs, et al.
Ugeskrift for Laeger|March 2, 1981
[Epidural morphine and respiratory improvement after upper laparotomy]J J Krintel, L Bitsch-Larsen, J Edlefsen, 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.
European Journal of Human Genetics : EJHG|November 26, 1999
Analysis of FMR1 (CGG)n alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from AsiaL A Larsen, J S Armstrong, K Grønskov, et al.
The British Journal of Dermatology|July 21, 2021
Evidence of gene-gene interaction in hidradenitis suppurativa: a nationwide registry study of Danish twinsR Kjaersgaard Andersen, S B Clemmensen, L A Larsen, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Delineation of an interstitial 9q22 deletion in basal cell nevus syndromeS E Boonen, D Stahl, S Kreiborg, et al.
American Journal of Medical Genetics. Part A|May 12, 2005
Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndromeZ Tümer, A M Henriksen, I Bache, et al.
American Journal of Medical Genetics|June 27, 2000
Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X allelesL A Larsen, J S Armstrong, K Grønskov, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Pharmaceutical Research|April 17, 2001
Hepatic disposition of fexofenadine: influence of the transport inhibitors erythromycin and dibromosulphothaleinR W Milne, L A Larsen, K L Jørgensen, 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.
The American Journal of Clinical Nutrition|July 1, 1991
Report on the Fourth Conference for Federally Supported Human Nutrition Research Units and CentersD E Danford, V S Hubbard, G F Combs, et al.
Ugeskrift for Laeger|March 2, 1981
[Epidural morphine and respiratory improvement after upper laparotomy]J J Krintel, L Bitsch-Larsen, J Edlefsen, 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.
European Journal of Human Genetics : EJHG|November 26, 1999
Analysis of FMR1 (CGG)n alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from AsiaL A Larsen, J S Armstrong, K Grønskov, et al.
The British Journal of Dermatology|July 21, 2021
Evidence of gene-gene interaction in hidradenitis suppurativa: a nationwide registry study of Danish twinsR Kjaersgaard Andersen, S B Clemmensen, L A Larsen, et al.
American Journal of Medical Genetics. Part A|February 4, 2005
Delineation of an interstitial 9q22 deletion in basal cell nevus syndromeS E Boonen, D Stahl, S Kreiborg, et al.
American Journal of Medical Genetics. Part A|May 12, 2005
Eponymous Jacobsen syndrome: mapping the breakpoints of the original family suggests an association between the distal 1.1 Mb of chromosome 21 and osteoporosis in Down syndromeZ Tümer, A M Henriksen, I Bache, et al.
American Journal of Medical Genetics|June 27, 2000
Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X allelesL A Larsen, J S Armstrong, K Grønskov, et al.
Pageof 4