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L Tranebjaerg

Showing results (91-100 of 107) with videos related to

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Ophthalmic Genetics|January 23, 2002
Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a geneL Tranebjaerg, P K Jensen, M Van Ghelue, et al.
American Journal of Human Genetics|April 16, 1998
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13P Pekkarinen, I Hovatta, P Hakola, et al.
Human Molecular Genetics|May 16, 1998
Non-disjunction of chromosome 18M Bugge, A Collins, M B Petersen, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Human Mutation|March 3, 1998
Constant denaturant gel electrophoresis (CDGE) in BRCA1 mutation screeningT I Andersen, H G Eiken, F Couch, et al.
American Journal of Medical Genetics|July 12, 1996
Seventh International Workshop on the Fragile X and X-linked Mental RetardationL Tranebjaerg, H A Lubs, M Borghgraef, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldA Lund, B Udd, V Juvonen, et al.
American Journal of Medical Genetics|April 20, 1999
Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997J J Holden, M Percy, D Allingham-Hawkins, et al.
Pageof 11

Showing results (91-100 of 107) with videos related to

Sort By:
Pageof 11
Ophthalmic Genetics|January 23, 2002
Neuronal cell death in the visual cortex is a prominent feature of the X-linked recessive mitochondrial deafness-dystonia syndrome caused by mutations in the TIMM8a geneL Tranebjaerg, P K Jensen, M Van Ghelue, et al.
American Journal of Human Genetics|April 16, 1998
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13P Pekkarinen, I Hovatta, P Hakola, et al.
Human Molecular Genetics|May 16, 1998
Non-disjunction of chromosome 18M Bugge, A Collins, M B Petersen, et al.
Human Molecular Genetics|November 5, 1997
IsK and KvLQT1: mutation in either of the two subunits of the slow component of the delayed rectifier potassium channel can cause Jervell and Lange-Nielsen syndromeJ Tyson, L Tranebjaerg, S Bellman, et al.
Genome Research|August 1, 1995
Genes and languages in Europe: an analysis of mitochondrial lineagesA Sajantila, P Lahermo, T Anttinen, et al.
Human Genetics|January 5, 2001
Mutational spectrum in the cardioauditory syndrome of Jervell and Lange-NielsenJ Tyson, L Tranebjaerg, M McEntagart, et al.
Human Mutation|March 3, 1998
Constant denaturant gel electrophoresis (CDGE) in BRCA1 mutation screeningT I Andersen, H G Eiken, F Couch, et al.
American Journal of Medical Genetics|July 12, 1996
Seventh International Workshop on the Fragile X and X-linked Mental RetardationL Tranebjaerg, H A Lubs, M Borghgraef, et al.
European Journal of Human Genetics : EJHG|July 4, 2001
Multiple founder effects in spinal and bulbar muscular atrophy (SBMA, Kennedy disease) around the worldA Lund, B Udd, V Juvonen, et al.
American Journal of Medical Genetics|April 20, 1999
Eighth International workshop on the fragile X syndrome and X-linked mental retardation, August 16-22, 1997J J Holden, M Percy, D Allingham-Hawkins, et al.
Pageof 11