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American Journal of Human Genetics
|
April 1, 1992
Mitochondrial ND-I mutation in Leber hereditary optic neuropathy
D R Johns
The New England Journal of Medicine
|
November 22, 1990
Improved molecular-genetic diagnosis of Leber's hereditary optic neuropathy
D R Johns
Genomics
|
October 1, 1989
Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNA
D R Johns, O Hurko
The New England Journal of Medicine
|
August 10, 1989
Dystrophin and Duchenne's muscular dystrophy
O Hurko, D R Johns
Neurologic Clinics
|
February 1, 1991
Neuro-ophthalmologic manifestations of mitochondrial DNA disorders: chronic progressive external ophthalmoplegia, Kearns-Sayre syndrome, and Leber's hereditary optic neuropathy
G Kosmorsky, D R Johns
Lancet (London, England)
|
April 13, 1991
Mitochondrial leucine tRNA mutation in neurological diseases
D R Johns, O Hurko
Seminars in Neurology
|
March 1, 1996
Clinical spectrum of mitochondrial diseases
R Fadic, D R Johns
Biochemical and Biophysical Research Communications
|
February 14, 1991
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
D R Johns, J Berman
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
September 1, 1994
Cuban epidemic optic neuropathy. Mitochondrial DNA analysis
D R Johns, A A Sadun
Biochemical and Biophysical Research Communications
|
October 29, 1993
Cytochrome c oxidase mutations in Leber hereditary optic neuropathy
D R Johns, M J Neufeld
Page
of 8
Search research articles
Search
Showing results (11-20 of 76) with videos related to
Sort By:
Page
of 8
American Journal of Human Genetics
|
April 1, 1992
Mitochondrial ND-I mutation in Leber hereditary optic neuropathy
D R Johns
The New England Journal of Medicine
|
November 22, 1990
Improved molecular-genetic diagnosis of Leber's hereditary optic neuropathy
D R Johns
Genomics
|
October 1, 1989
Preferential amplification and molecular characterization of junction sequences of a pathogenetic deletion in human mitochondrial DNA
D R Johns, O Hurko
The New England Journal of Medicine
|
August 10, 1989
Dystrophin and Duchenne's muscular dystrophy
O Hurko, D R Johns
Neurologic Clinics
|
February 1, 1991
Neuro-ophthalmologic manifestations of mitochondrial DNA disorders: chronic progressive external ophthalmoplegia, Kearns-Sayre syndrome, and Leber's hereditary optic neuropathy
G Kosmorsky, D R Johns
Lancet (London, England)
|
April 13, 1991
Mitochondrial leucine tRNA mutation in neurological diseases
D R Johns, O Hurko
Seminars in Neurology
|
March 1, 1996
Clinical spectrum of mitochondrial diseases
R Fadic, D R Johns
Biochemical and Biophysical Research Communications
|
February 14, 1991
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy
D R Johns, J Berman
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society
|
September 1, 1994
Cuban epidemic optic neuropathy. Mitochondrial DNA analysis
D R Johns, A A Sadun
Biochemical and Biophysical Research Communications
|
October 29, 1993
Cytochrome c oxidase mutations in Leber hereditary optic neuropathy
D R Johns, M J Neufeld
Page
of 8