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Showing results (61-70 of 69) with videos related to

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The American Journal of Tropical Medicine and Hygiene|March 1, 1992
Antibodies to a recombinant glutamate-rich Plasmodium falciparum protein: evidence for protection of individuals living in a holoendemic area of LiberiaB Hogh, E Petersen, M Dziegiel, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Structure of a human gastrin geneO Wiborg, L Berglund, E Boel, 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.
FEMS Immunology and Medical Microbiology|February 1, 1995
Development of a PCR-based technique for detection of Helicobacter pyloriA C Thoreson, M B Borre, L P Andersen, 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.
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.
Clinical Genetics|March 29, 2000
Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2L A Larsen, I H Svendsen, A M Jensen, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
Pageof 7

Showing results (61-70 of 69) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 69 results.
The American Journal of Tropical Medicine and Hygiene|March 1, 1992
Antibodies to a recombinant glutamate-rich Plasmodium falciparum protein: evidence for protection of individuals living in a holoendemic area of LiberiaB Hogh, E Petersen, M Dziegiel, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Structure of a human gastrin geneO Wiborg, L Berglund, E Boel, 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.
FEMS Immunology and Medical Microbiology|February 1, 1995
Development of a PCR-based technique for detection of Helicobacter pyloriA C Thoreson, M B Borre, L P Andersen, 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.
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.
Clinical Genetics|March 29, 2000
Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2L A Larsen, I H Svendsen, A M Jensen, et al.
Journal of Medical Genetics|December 19, 2001
Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populationsP S Andersen, O Havndrup, H Bundgaard, et al.
Pageof 7