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E K Nikoskelainen

Showing results (1-10 of 12) with videos related to

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American Journal of Human Genetics|August 1, 1989
Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphismJ Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics|December 1, 1988
Human mitochondrial DNA types in FinlandJ Vilkki, M L Savontaus, E K Nikoskelainen
American Journal of Human Genetics|July 1, 1990
Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathyJ Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics|June 1, 1989
Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathyJ Vilkki, M L Savontaus, H Kalimo, et al.
Lancet (London, England)|September 24, 1994
Pre-excitation syndrome in Leber's hereditary optic neuropathyE K Nikoskelainen, M L Savontaus, K Huoponen, et al.
Genomics|November 1, 1990
Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, M L Savontaus, et al.
American Journal of Human Genetics|March 1, 1991
Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7J Vilkki, J Ott, M L Savontaus, et al.
American Journal of Human Genetics|June 1, 1991
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, P Aula, et al.
Ophthalmology|March 1, 1996
Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutationsE K Nikoskelainen, K Huoponen, V Juvonen, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1987
Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigreesE K Nikoskelainen, M L Savontaus, O P Wanne, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
American Journal of Human Genetics|August 1, 1989
Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphismJ Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics|December 1, 1988
Human mitochondrial DNA types in FinlandJ Vilkki, M L Savontaus, E K Nikoskelainen
American Journal of Human Genetics|July 1, 1990
Segregation of mitochondrial genomes in a heteroplasmic lineage with Leber hereditary optic neuroretinopathyJ Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics|June 1, 1989
Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathyJ Vilkki, M L Savontaus, H Kalimo, et al.
Lancet (London, England)|September 24, 1994
Pre-excitation syndrome in Leber's hereditary optic neuropathyE K Nikoskelainen, M L Savontaus, K Huoponen, et al.
Genomics|November 1, 1990
Analysis of mitochondrial ND4 gene DNA sequence in Finnish families with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, M L Savontaus, et al.
American Journal of Human Genetics|March 1, 1991
Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7J Vilkki, J Ott, M L Savontaus, et al.
American Journal of Human Genetics|June 1, 1991
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathyK Huoponen, J Vilkki, P Aula, et al.
Ophthalmology|March 1, 1996
Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutationsE K Nikoskelainen, K Huoponen, V Juvonen, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|May 1, 1987
Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigreesE K Nikoskelainen, M L Savontaus, O P Wanne, et al.
Pageof 2