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V Monsalve

Showing results (31-40 of 37) with videos related to

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Revista Medica De Chile|April 1, 1989
[Von Willebrand's disease in the IX Region of Chile]M E Cabrera, C G Artigas, E Páez, et al.
Atherosclerosis|March 1, 1988
DNA polymorphisms of the gene for apolipoprotein B in patients with peripheral arterial diseaseM V Monsalve, R Young, J Jobsis, et al.
American Journal of Physical Anthropology|June 22, 2000
Beta-globin gene cluster haplotypes in two North American indigenous populationsV S Mattevi, M Fiegenbaum, F M Salzano, et al.
Annals of Human Genetics|August 14, 2003
Methylenetetrahydrofolate reductase (MTHFR) allele frequencies in AmerindiansM V Monsalve, F M Salzano, J L Rupert, et al.
The New England Journal of Medicine|June 20, 1991
A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French CanadiansY Ma, H E Henderson, V Murthy, et al.
The Journal of Clinical Investigation|September 1, 1990
A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestriesM V Monsalve, H Henderson, G Roederer, et al.
The Journal of Clinical Investigation|June 1, 1991
Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric originH E Henderson, Y Ma, M F Hassan, et al.
Pageof 4

Showing results (31-40 of 37) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 37 results.
Revista Medica De Chile|April 1, 1989
[Von Willebrand's disease in the IX Region of Chile]M E Cabrera, C G Artigas, E Páez, et al.
Atherosclerosis|March 1, 1988
DNA polymorphisms of the gene for apolipoprotein B in patients with peripheral arterial diseaseM V Monsalve, R Young, J Jobsis, et al.
American Journal of Physical Anthropology|June 22, 2000
Beta-globin gene cluster haplotypes in two North American indigenous populationsV S Mattevi, M Fiegenbaum, F M Salzano, et al.
Annals of Human Genetics|August 14, 2003
Methylenetetrahydrofolate reductase (MTHFR) allele frequencies in AmerindiansM V Monsalve, F M Salzano, J L Rupert, et al.
The New England Journal of Medicine|June 20, 1991
A mutation in the human lipoprotein lipase gene as the most common cause of familial chylomicronemia in French CanadiansY Ma, H E Henderson, V Murthy, et al.
The Journal of Clinical Investigation|September 1, 1990
A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestriesM V Monsalve, H Henderson, G Roederer, et al.
The Journal of Clinical Investigation|June 1, 1991
Amino acid substitution (Ile194----Thr) in exon 5 of the lipoprotein lipase gene causes lipoprotein lipase deficiency in three unrelated probands. Support for a multicentric originH E Henderson, Y Ma, M F Hassan, et al.
Pageof 4