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Clinical Genetics|April 1, 1991

Within-individual variation in serum cholesterol levels: association with DNA polymorphisms at the apolipoprotein B and AI-CIII-AIV loci in patients with peripheral arterial diseaseM V Monsalve, D Robinson, N E Woolcock, et al.

Annals of Human Genetics|August 28, 2003

Selective pressure has not acted against hypercoagulability alleles in high-altitude AmerindiansJ L Rupert, M V Monsalve, K K Kidd, et al.

Annals of Human Genetics|January 31, 2003

Genetic polymorphisms in the Renin-Angiotensin system in high-altitude and low-altitude Native American populationsJ L Rupert, K K Kidd, L E Norman, et al.

Clinical Science (London, England : 1979)|February 1, 1989

Study of DNA polymorphisms of the apolipoprotein AI-CIII-AIV gene cluster in patients with peripheral arterial diseaseM V Monsalve, R Young, S A Wiseman, 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.

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

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You have reached the last page of results.This site can display upto 20 results.

Clinical Genetics|April 1, 1991

Within-individual variation in serum cholesterol levels: association with DNA polymorphisms at the apolipoprotein B and AI-CIII-AIV loci in patients with peripheral arterial diseaseM V Monsalve, D Robinson, N E Woolcock, et al.

Annals of Human Genetics|August 28, 2003

Selective pressure has not acted against hypercoagulability alleles in high-altitude AmerindiansJ L Rupert, M V Monsalve, K K Kidd, et al.

Annals of Human Genetics|January 31, 2003

Genetic polymorphisms in the Renin-Angiotensin system in high-altitude and low-altitude Native American populationsJ L Rupert, K K Kidd, L E Norman, et al.

Clinical Science (London, England : 1979)|February 1, 1989

Study of DNA polymorphisms of the apolipoprotein AI-CIII-AIV gene cluster in patients with peripheral arterial diseaseM V Monsalve, R Young, S A Wiseman, 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.

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