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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 Liberia
B 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 gene
O 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 chain
H 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 Asia
L 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 pylori
A 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 alleles
L 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 syndrome
L 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 KCNH2
L 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 populations
P S Andersen, O Havndrup, H Bundgaard, et al.
Page
of 7
Search research articles
Search
Showing results (61-70 of 69) with videos related to
Sort By:
Page
of 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 Liberia
B 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 gene
O 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 chain
H 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 Asia
L 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 pylori
A 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 alleles
L 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 syndrome
L 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 KCNH2
L 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 populations
P S Andersen, O Havndrup, H Bundgaard, et al.
Page
of 7