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J T Epplen

Showing results (241-250 of 365) with videos related to

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Nucleic Acids Research|December 11, 1989
Polymorphic simple GATA/GACA repeats in plant genomesK Weising, F Weigand, A J Driesel, et al.
Pneumologie (Stuttgart, Germany)|January 13, 2009
[The genetics of chronic obstructive pulmonary disease]U Arinir, S Hoffjan, H Knoop, et al.
European Journal of Pediatrics|July 31, 2001
Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient careU Schara, M Gencik, J Mortier, et al.
Journal of Dermatological Science|June 16, 2009
Analysis of variation in the IL7RA and IL2RA genes in atopic dermatitisS Hoffjan, J Beygo, D A Akkad, et al.
Journal of Neurosurgery|April 8, 1999
Lhermitte-Duclos disease as a component of Cowden's syndrome. Case report and review of the literatureR Koch, M Scholz, M R Nelen, et al.
Molecular Ecology|March 29, 2000
Novel polymorphic microsatellite loci isolated from the yellow waterlily, Nuphar luteaN J Ouborg, W P Goodall-Copestake, P Saumitou-Laprade, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 31, 2002
Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patientsP Wintermeyer, O Riess, L Schöls, et al.
Scandinavian Journal of Immunology|February 1, 1987
Loss of antigen recognition and impaired cytolytic function in most hybrids between cytotoxic T cells and BW5147D Woodland, D L Janković, H U Weltzien, et al.
Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.
Journal of Medical Genetics|February 4, 2005
Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndromeM Meins, J Lehmann, F Gerresheim, et al.
Pageof 37

Showing results (241-250 of 365) with videos related to

Sort By:
Pageof 37
Nucleic Acids Research|December 11, 1989
Polymorphic simple GATA/GACA repeats in plant genomesK Weising, F Weigand, A J Driesel, et al.
Pneumologie (Stuttgart, Germany)|January 13, 2009
[The genetics of chronic obstructive pulmonary disease]U Arinir, S Hoffjan, H Knoop, et al.
European Journal of Pediatrics|July 31, 2001
Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient careU Schara, M Gencik, J Mortier, et al.
Journal of Dermatological Science|June 16, 2009
Analysis of variation in the IL7RA and IL2RA genes in atopic dermatitisS Hoffjan, J Beygo, D A Akkad, et al.
Journal of Neurosurgery|April 8, 1999
Lhermitte-Duclos disease as a component of Cowden's syndrome. Case report and review of the literatureR Koch, M Scholz, M R Nelen, et al.
Molecular Ecology|March 29, 2000
Novel polymorphic microsatellite loci isolated from the yellow waterlily, Nuphar luteaN J Ouborg, W P Goodall-Copestake, P Saumitou-Laprade, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 31, 2002
Mutation analysis and association studies of nuclear factor-kappaB1 in sporadic Parkinson's disease patientsP Wintermeyer, O Riess, L Schöls, et al.
Scandinavian Journal of Immunology|February 1, 1987
Loss of antigen recognition and impaired cytolytic function in most hybrids between cytotoxic T cells and BW5147D Woodland, D L Janković, H U Weltzien, et al.
Human Genetics|September 1, 1989
RFLP-discordance within the human phenylalanine hydroxylase locusO Riess, A Michel, W Berger, et al.
Journal of Medical Genetics|February 4, 2005
Submicroscopic duplication in Xq28 causes increased expression of the MECP2 gene in a boy with severe mental retardation and features of Rett syndromeM Meins, J Lehmann, F Gerresheim, et al.
Pageof 37