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Mutation Research
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February 7, 2001
Improved bacterial SOS promoter∷lux fusions for genotoxicity detection
Y Davidov, R Rozen, D R Smulski, et al.
Circulation
|
January 1, 1996
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations
P F Jacques, A G Bostom, R R Williams, et al.
Circulation
|
November 15, 1996
Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians
J Ma, M J Stampfer, C H Hennekens, et al.
The New England Journal of Medicine
|
November 6, 1986
Prenatal diagnosis of ornithine transcarbamylase deficiency with use of DNA polymorphisms
J Fox, A M Hack, W A Fenton, et al.
Circulation
|
November 1, 1996
Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation
P M Gallagher, R Meleady, D C Shields, et al.
American Journal of Medical Genetics
|
February 1, 1992
Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis
R Rozen, M De Braekeleer, J Daigneault, et al.
Human Molecular Genetics
|
December 1, 1996
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders
D Leclerc, E Campeau, P Goyette, et al.
Cancer Research
|
March 15, 1997
Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer
J Ma, M J Stampfer, E Giovannucci, et al.
American Journal of Human Genetics
|
August 10, 2000
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
C A Hobbs, S L Sherman, P Yi, et al.
American Journal of Human Genetics
|
October 1, 1990
Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian families
R Rozen, R H Schwartz, B C Hilman, et al.
Page
of 16
Search research articles
Search
Showing results (131-140 of 154) with videos related to
Sort By:
Page
of 16
Mutation Research
|
February 7, 2001
Improved bacterial SOS promoter∷lux fusions for genotoxicity detection
Y Davidov, R Rozen, D R Smulski, et al.
Circulation
|
January 1, 1996
Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations
P F Jacques, A G Bostom, R R Williams, et al.
Circulation
|
November 15, 1996
Methylenetetrahydrofolate reductase polymorphism, plasma folate, homocysteine, and risk of myocardial infarction in US physicians
J Ma, M J Stampfer, C H Hennekens, et al.
The New England Journal of Medicine
|
November 6, 1986
Prenatal diagnosis of ornithine transcarbamylase deficiency with use of DNA polymorphisms
J Fox, A M Hack, W A Fenton, et al.
Circulation
|
November 1, 1996
Homocysteine and risk of premature coronary heart disease. Evidence for a common gene mutation
P M Gallagher, R Meleady, D C Shields, et al.
American Journal of Medical Genetics
|
February 1, 1992
Cystic fibrosis mutations in French Canadians: three CFTR mutations are relatively frequent in a Quebec population with an elevated incidence of cystic fibrosis
R Rozen, M De Braekeleer, J Daigneault, et al.
Human Molecular Genetics
|
December 1, 1996
Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders
D Leclerc, E Campeau, P Goyette, et al.
Cancer Research
|
March 15, 1997
Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer
J Ma, M J Stampfer, E Giovannucci, et al.
American Journal of Human Genetics
|
August 10, 2000
Polymorphisms in genes involved in folate metabolism as maternal risk factors for Down syndrome
C A Hobbs, S L Sherman, P Yi, et al.
American Journal of Human Genetics
|
October 1, 1990
Cystic fibrosis mutations in North American populations of French ancestry: analysis of Quebec French-Canadian and Louisiana Acadian families
R Rozen, R H Schwartz, B C Hilman, et al.
Page
of 16