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P de Knijff

Showing results (21-30 of 95) with videos related to

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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 deafnessJ 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 populationsT 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 residueM 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 populationsL 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 levelsM 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 diseaseC 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 StudyL Tiret, P de Knijff, H J Menzel, et al.
Lancet (London, England)|July 4, 1992
Fibrinogen genes and peripheral arterial diseaseP 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 familyM 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 SaamiP Lahermo, M L Savontaus, P Sistonen, et al.
Pageof 10

Showing results (21-30 of 95) with videos related to

Sort By:
Pageof 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 deafnessJ 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 populationsT 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 residueM 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 populationsL 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 levelsM 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 diseaseC 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 StudyL Tiret, P de Knijff, H J Menzel, et al.
Lancet (London, England)|July 4, 1992
Fibrinogen genes and peripheral arterial diseaseP 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 familyM 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 SaamiP Lahermo, M L Savontaus, P Sistonen, et al.
Pageof 10