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Archives of Physiology and Biochemistry
|
September 11, 2002
A case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness
J A Maassen, S Biberoglu, L M 't Hart, et al.
Human Biology
|
November 24, 1998
Different patterns of variation at the X- and Y-chromosome-linked microsatellite loci DXYS156X and DXYS156Y in human populations
T Karafet, P de Knijff, E Wood, et al.
Clinical Genetics
|
November 1, 1987
Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residue
M Smit, P de Knijff, R R Frants, et al.
Human Molecular Genetics
|
July 1, 1996
Analysis of molecular variance (AMOVA) of Y-chromosome-specific microsatellites in two closely related human populations
L Roewer, M Kayser, P Dieltjes, et al.
Human Genetics
|
November 1, 1988
Apolipoprotein E polymorphism in The Netherlands and its effect on plasma lipid and apolipoprotein levels
M Smit, P de Knijff, M Rosseneu, et al.
BMJ (Clinical Research Ed.)
|
March 11, 1995
Apolipoprotein E genotype and association between smoking and early onset Alzheimer's disease
C M van Duijn, L M Havekes, C Van Broeckhoven, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
October 1, 1994
ApoE polymorphism and predisposition to coronary heart disease in youths of different European populations. The EARS Study. European Atherosclerosis Research Study
L Tiret, P de Knijff, H J Menzel, et al.
Lancet (London, England)
|
July 4, 1992
Fibrinogen genes and peripheral arterial disease
P de Knijff, A C de Bart, R R Frants, et al.
Human Heredity
|
January 1, 1988
Rare apolipoprotein E variant cosegregating with a unique APOE-C1-C2 haplotype in a normolipidemic family
M Smit, P de Knijff, A Sijts, et al.
European Journal of Human Genetics : EJHG
|
June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami
P Lahermo, M L Savontaus, P Sistonen, et al.
Page
of 10
Search research articles
Search
Showing results (21-30 of 95) with videos related to
Sort By:
Page
of 10
Archives of Physiology and Biochemistry
|
September 11, 2002
A case of a de novo A3243G mutation in mitochondrial DNA in a patient with diabetes and deafness
J A Maassen, S Biberoglu, L M 't Hart, et al.
Human Biology
|
November 24, 1998
Different patterns of variation at the X- and Y-chromosome-linked microsatellite loci DXYS156X and DXYS156Y in human populations
T Karafet, P de Knijff, E Wood, et al.
Clinical Genetics
|
November 1, 1987
Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residue
M Smit, P de Knijff, R R Frants, et al.
Human Molecular Genetics
|
July 1, 1996
Analysis of molecular variance (AMOVA) of Y-chromosome-specific microsatellites in two closely related human populations
L Roewer, M Kayser, P Dieltjes, et al.
Human Genetics
|
November 1, 1988
Apolipoprotein E polymorphism in The Netherlands and its effect on plasma lipid and apolipoprotein levels
M Smit, P de Knijff, M Rosseneu, et al.
BMJ (Clinical Research Ed.)
|
March 11, 1995
Apolipoprotein E genotype and association between smoking and early onset Alzheimer's disease
C M van Duijn, L M Havekes, C Van Broeckhoven, et al.
Arteriosclerosis and Thrombosis : a Journal of Vascular Biology
|
October 1, 1994
ApoE polymorphism and predisposition to coronary heart disease in youths of different European populations. The EARS Study. European Atherosclerosis Research Study
L Tiret, P de Knijff, H J Menzel, et al.
Lancet (London, England)
|
July 4, 1992
Fibrinogen genes and peripheral arterial disease
P de Knijff, A C de Bart, R R Frants, et al.
Human Heredity
|
January 1, 1988
Rare apolipoprotein E variant cosegregating with a unique APOE-C1-C2 haplotype in a normolipidemic family
M Smit, P de Knijff, A Sijts, et al.
European Journal of Human Genetics : EJHG
|
June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami
P Lahermo, M L Savontaus, P Sistonen, et al.
Page
of 10