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Showing results (121-130 of 282) with videos related to

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European Archives of Psychiatry and Clinical Neuroscience|September 29, 2000
hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophreniaG Stöber, J Meyer, I Nanda, et al.
European Journal of Human Genetics : EJHG|November 10, 2016
Klüver-Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C)Hao Hu, Christoph Hübner, Zoltan Lukacs, et al.
European Journal of Human Genetics : EJHG|April 22, 2004
Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemiaJohannes Dietter, Alexander Spiegel, Dieter an Mey, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Localisation of a Fanconi anaemia gene to chromosome 9pK Saar, D Schindler, R D Wegner, et al.
Thrombosis and Haemostasis|November 8, 2005
VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulationChristof Geisen, Matthias Watzka, Katja Sittinger, et al.
Epilepsy Research|February 26, 1998
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsyT Sander, C Peters, D Janz, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 12, 2002
Evolutionary conserved microsatellites in the promoter region of the 5-hydroxytryptamine receptor 2C gene (HTR2C) are not associated with bipolar disorder in femalesJ Meyer, W Saam, R Mössner, et al.
The Journal of Investigative Dermatology|April 14, 1999
Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium testN Jacob, F Rüschendorf, M Schmitt-Egenolf, et al.
Cell Cycle (Georgetown, Tex.)|April 3, 2014
Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutationsHao Hu, Vanessa Suckow, Luciana Musante, et al.
The Journal of Allergy and Clinical Immunology|May 8, 2004
Multilocus haplotype analyses reveal association between 5 novel IL-15 polymorphisms and asthmaThorsten Kurz, Konstantin Strauch, Henriette Dietrich, et al.
Pageof 29

Showing results (121-130 of 282) with videos related to

Sort By:
Pageof 29
European Archives of Psychiatry and Clinical Neuroscience|September 29, 2000
hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophreniaG Stöber, J Meyer, I Nanda, et al.
European Journal of Human Genetics : EJHG|November 10, 2016
Klüver-Bucy syndrome associated with a recessive variant in HGSNAT in two siblings with Mucopolysaccharidosis type IIIC (Sanfilippo C)Hao Hu, Christoph Hübner, Zoltan Lukacs, et al.
European Journal of Human Genetics : EJHG|April 22, 2004
Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemiaJohannes Dietter, Alexander Spiegel, Dieter an Mey, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Localisation of a Fanconi anaemia gene to chromosome 9pK Saar, D Schindler, R D Wegner, et al.
Thrombosis and Haemostasis|November 8, 2005
VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulationChristof Geisen, Matthias Watzka, Katja Sittinger, et al.
Epilepsy Research|February 26, 1998
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsyT Sander, C Peters, D Janz, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|July 12, 2002
Evolutionary conserved microsatellites in the promoter region of the 5-hydroxytryptamine receptor 2C gene (HTR2C) are not associated with bipolar disorder in femalesJ Meyer, W Saam, R Mössner, et al.
The Journal of Investigative Dermatology|April 14, 1999
Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium testN Jacob, F Rüschendorf, M Schmitt-Egenolf, et al.
Cell Cycle (Georgetown, Tex.)|April 3, 2014
Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutationsHao Hu, Vanessa Suckow, Luciana Musante, et al.
The Journal of Allergy and Clinical Immunology|May 8, 2004
Multilocus haplotype analyses reveal association between 5 novel IL-15 polymorphisms and asthmaThorsten Kurz, Konstantin Strauch, Henriette Dietrich, et al.
Pageof 29