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T Wienker

Showing results (21-30 of 35) with videos related to

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Human Genetics|May 1, 1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19M Koch, H Harley, M Sarfarazi, et al.
Annals of Human Genetics|March 30, 2000
Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor geneJ Erdmann, K Riedel, K Rohde, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|September 20, 2005
[Y402H polymorphism in complement factor H and age-related macula degeneration (AMD)]H P N Scholl, B H F Weber, M M Nöthen, et al.
American Journal of Human Genetics|December 5, 1998
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene clusterM Vollmer, M Jung, F Rüschendorf, et al.
American Journal of Human Genetics|April 17, 1999
Quantitative analysis of survival motor neuron copies: identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counselingB Wirth, M Herz, A Wetter, et al.
The American Journal of Cardiology|August 1, 1996
Angiotensin-converting enzyme and heart chymase gene polymorphisms in hypertrophic cardiomyopathyA Pfeufer, K J Osterziel, H Urata, et al.
Clinical Genetics|March 1, 1985
Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosomeA Gal, C Stolzenberger, T Wienker, 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.
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.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
Human Genetics|May 1, 1989
Myotonia congenita (Thomsen's disease) excluded from the region of the myotonic dystrophy locus on chromosome 19M Koch, H Harley, M Sarfarazi, et al.
Annals of Human Genetics|March 30, 2000
Characterization of polymorphisms in the promoter of the human angiotensin II subtype 1 (AT1) receptor geneJ Erdmann, K Riedel, K Rohde, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|September 20, 2005
[Y402H polymorphism in complement factor H and age-related macula degeneration (AMD)]H P N Scholl, B H F Weber, M M Nöthen, et al.
American Journal of Human Genetics|December 5, 1998
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene clusterM Vollmer, M Jung, F Rüschendorf, et al.
American Journal of Human Genetics|April 17, 1999
Quantitative analysis of survival motor neuron copies: identification of subtle SMN1 mutations in patients with spinal muscular atrophy, genotype-phenotype correlation, and implications for genetic counselingB Wirth, M Herz, A Wetter, et al.
The American Journal of Cardiology|August 1, 1996
Angiotensin-converting enzyme and heart chymase gene polymorphisms in hypertrophic cardiomyopathyA Pfeufer, K J Osterziel, H Urata, et al.
Clinical Genetics|March 1, 1985
Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosomeA Gal, C Stolzenberger, T Wienker, 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.
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.
Pageof 4