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American Journal of Human Genetics
|
August 1, 1989
Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism
J Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics
|
December 1, 1988
Human mitochondrial DNA types in Finland
J 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 neuroretinopathy
J Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics
|
June 1, 1989
Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy
J Vilkki, M L Savontaus, H Kalimo, et al.
Lancet (London, England)
|
September 24, 1994
Pre-excitation syndrome in Leber's hereditary optic neuropathy
E 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 neuroretinopathy
K 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 DXS7
J 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 neuroretinopathy
K Huoponen, J Vilkki, P Aula, et al.
Ophthalmology
|
March 1, 1996
Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations
E 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 pedigrees
E K Nikoskelainen, M L Savontaus, O P Wanne, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 12) with videos related to
Sort By:
Page
of 2
American Journal of Human Genetics
|
August 1, 1989
Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism
J Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics
|
December 1, 1988
Human mitochondrial DNA types in Finland
J 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 neuroretinopathy
J Vilkki, M L Savontaus, E K Nikoskelainen
Human Genetics
|
June 1, 1989
Mitochondrial DNA polymorphism in Finnish families with Leber's hereditary optic neuroretinopathy
J Vilkki, M L Savontaus, H Kalimo, et al.
Lancet (London, England)
|
September 24, 1994
Pre-excitation syndrome in Leber's hereditary optic neuropathy
E 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 neuroretinopathy
K 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 DXS7
J 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 neuroretinopathy
K Huoponen, J Vilkki, P Aula, et al.
Ophthalmology
|
March 1, 1996
Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations
E 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 pedigrees
E K Nikoskelainen, M L Savontaus, O P Wanne, et al.
Page
of 2