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American Journal of Human Genetics
|
May 1, 1993
Characterization of five new mutants in the carboxyl-terminal domain of human apolipoprotein E: no cosegregation with severe hyperlipidemia
A M van den Maagdenberg, W Weng, I H de Bruijn, et al.
Tissue Antigens
|
November 5, 1998
Selective co-evolution of the D6STNFa microsatellite region with HLA class I and II loci
P H Moghaddam, P de Knijff, R F Schipper, et al.
Human Molecular Genetics
|
February 3, 2000
A polymorphic L1 retroposon insertion in the centromere of the human Y chromosome
F R Santos, A Pandya, M Kayser, et al.
Journal of Lipid Research
|
January 1, 1990
Genetic heterogeneity in familial dysbetalipoproteinemia. The E2(lys146----gln) variant results in a dominant mode of inheritance
M Smit, P de Knijff, E van der Kooij-Meijs, et al.
American Journal of Human Genetics
|
March 3, 1999
Ancestral Asian source(s) of new world Y-chromosome founder haplotypes
T M Karafet, S L Zegura, O Posukh, et al.
Journal of Neural Transmission. Supplementum
|
August 13, 1998
Apolipoprotein E genotype, atherosclerosis, and cognitive decline: the Rotterdam Study
A J Slooter, C M van Duijn, M L Bots, et al.
Scientific Reports
|
August 5, 2016
Phylogeographic Patterns in Africa and High Resolution Delineation of Genetic Clades in the Lion (Panthera leo)
L D Bertola, H Jongbloed, K J van der Gaag, et al.
International Journal of Legal Medicine
|
August 18, 2001
DNA commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs
P Gill, C Brenner, B Brinkmann, et al.
Forensic Science International
|
December 14, 2001
DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs
P Gill, C Brenner, B Brinkmann, et al.
Disease Markers
|
January 6, 2011
Matrix metalloproteinases 2 and 3 gene polymorphisms and the risk of target vessel revascularization after percutaneous coronary intervention: Is there still room for determining genetic variation of MMPs for assessment of an increased risk of restenosis?
J J W Verschuren, M L Sampietro, D Pons, et al.
Page
of 10
Search research articles
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Showing results (81-90 of 95) with videos related to
Sort By:
Page
of 10
American Journal of Human Genetics
|
May 1, 1993
Characterization of five new mutants in the carboxyl-terminal domain of human apolipoprotein E: no cosegregation with severe hyperlipidemia
A M van den Maagdenberg, W Weng, I H de Bruijn, et al.
Tissue Antigens
|
November 5, 1998
Selective co-evolution of the D6STNFa microsatellite region with HLA class I and II loci
P H Moghaddam, P de Knijff, R F Schipper, et al.
Human Molecular Genetics
|
February 3, 2000
A polymorphic L1 retroposon insertion in the centromere of the human Y chromosome
F R Santos, A Pandya, M Kayser, et al.
Journal of Lipid Research
|
January 1, 1990
Genetic heterogeneity in familial dysbetalipoproteinemia. The E2(lys146----gln) variant results in a dominant mode of inheritance
M Smit, P de Knijff, E van der Kooij-Meijs, et al.
American Journal of Human Genetics
|
March 3, 1999
Ancestral Asian source(s) of new world Y-chromosome founder haplotypes
T M Karafet, S L Zegura, O Posukh, et al.
Journal of Neural Transmission. Supplementum
|
August 13, 1998
Apolipoprotein E genotype, atherosclerosis, and cognitive decline: the Rotterdam Study
A J Slooter, C M van Duijn, M L Bots, et al.
Scientific Reports
|
August 5, 2016
Phylogeographic Patterns in Africa and High Resolution Delineation of Genetic Clades in the Lion (Panthera leo)
L D Bertola, H Jongbloed, K J van der Gaag, et al.
International Journal of Legal Medicine
|
August 18, 2001
DNA commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs
P Gill, C Brenner, B Brinkmann, et al.
Forensic Science International
|
December 14, 2001
DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs
P Gill, C Brenner, B Brinkmann, et al.
Disease Markers
|
January 6, 2011
Matrix metalloproteinases 2 and 3 gene polymorphisms and the risk of target vessel revascularization after percutaneous coronary intervention: Is there still room for determining genetic variation of MMPs for assessment of an increased risk of restenosis?
J J W Verschuren, M L Sampietro, D Pons, et al.
Page
of 10