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Proceedings of the National Academy of Sciences of the United States of America|October 1, 1989
Directly repeated sequences associated with pathogenic mitochondrial DNA deletionsD R Johns, S L Rutledge, O C Stine, et al.Journal of Inherited Metabolic Disease|September 14, 2002
Sequence analysis of Hungarian LHON patients not carrying the common primary mutationsJ Horvath, R Horvath, V Karcagi, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 29, 1999
Dystonia as a presenting feature of the 3243 mitochondrial DNA mutationL Sudarsky, G M Plotkin, E L Logigian, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|November 1, 1993
Heteroplasmy in Leber's hereditary optic neuropathyK H Smith, D R Johns, K L Heher, et al.Ophthalmology|July 1, 1993
Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutationD R Johns, K H Smith, P J Savino, et al.AJNR. American Journal of Neuroradiology|May 1, 1995
MR of the brain in mitochondrial myopathyS H Wray, J M Provenzale, D R Johns, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|April 1, 1993
Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutationD R Johns, K L Heher, N R Miller, et al.American Journal of Human Genetics|June 1, 1989
Dystrophin analysis in clonal myoblasts derived from a Duchenne muscular dystrophy carrierO Hurko, E P Hoffman, L McKee, et al.Eye (London, England)|May 8, 2001
Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy populationC F Dogulu, T Kansu, V Seyrantepe, et al.Genomics|September 19, 1998
Mutational scanning of mitochondrial DNA by two-dimensional electrophoresisN J van Orsouw, X Zhang, J Y Wei, et al.Pageof 6