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Wienker

Showing results (131-140 of 282) with videos related to

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Human Genetics|July 1, 1988
Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14S Bissbort, H W Hitzeroth, D P du Wentzel, et al.
Human Genetics|January 24, 1998
Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mappingM W Laass, H C Hennies, S Preis, et al.
American Journal of Human Genetics|August 1, 1997
Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakersM Starfield, H C Hennies, M Jung, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 18, 2007
Increased frequency of the CTLA-4 49 A/G polymorphism in patients with acquired haemophilia A compared to healthy controlsA Pavlova, A Diaz-Lacava, H Zeitler, et al.
Annals of Neurology|August 1, 1995
The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1"T Sander, T Hildmann, D Janz, et al.
The British Journal of Dermatology|August 23, 2003
Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasisP Hensen, K Asadullah, C Windemuth, et al.
Tissue Antigens|September 15, 2001
Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw*0602-B*5701 in German familiesM Schmitt-Egenolf, C Windemuth, H C Hennies, et al.
American Journal of Medical Genetics|July 25, 1997
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphismT Sander, T Hildmann, R Kretz, et al.
American Journal of Medical Genetics|July 18, 2000
Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13G Stöber, J Meyer, I Nanda, et al.
American Journal of Human Genetics|July 6, 2000
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36K Bosse, R C Betz, Y A Lee, et al.
Pageof 29

Showing results (131-140 of 282) with videos related to

Sort By:
Pageof 29
Human Genetics|July 1, 1988
Linkage between the variegate porphyria (VP) and the alpha-1-antitrypsin (PI) genes on human chromosome 14S Bissbort, H W Hitzeroth, D P du Wentzel, et al.
Human Genetics|January 24, 1998
Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mappingM W Laass, H C Hennies, S Preis, et al.
American Journal of Human Genetics|August 1, 1997
Localization of the gene causing keratolytic winter erythema to chromosome 8p22-p23, and evidence for a founder effect in South African Afrikaans-speakersM Starfield, H C Hennies, M Jung, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|December 18, 2007
Increased frequency of the CTLA-4 49 A/G polymorphism in patients with acquired haemophilia A compared to healthy controlsA Pavlova, A Diaz-Lacava, H Zeitler, et al.
Annals of Neurology|August 1, 1995
The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1"T Sander, T Hildmann, D Janz, et al.
The British Journal of Dermatology|August 23, 2003
Interleukin-10 promoter polymorphism IL10.G and familial early onset psoriasisP Hensen, K Asadullah, C Windemuth, et al.
Tissue Antigens|September 15, 2001
Comparative association analysis reveals that corneodesmosin is more closely associated with psoriasis than HLA-Cw*0602-B*5701 in German familiesM Schmitt-Egenolf, C Windemuth, H C Hennies, et al.
American Journal of Medical Genetics|July 25, 1997
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphismT Sander, T Hildmann, R Kretz, et al.
American Journal of Medical Genetics|July 18, 2000
Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13G Stöber, J Meyer, I Nanda, et al.
American Journal of Human Genetics|July 6, 2000
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36K Bosse, R C Betz, Y A Lee, et al.
Pageof 29