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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|April 25, 2006
The modulation of skeletal muscle glycosylation as a potential therapeutic intervention in muscular dystrophiesM Brockington, F MuntoniBritish Journal of Haematology|June 1, 1995
Pearson's marrow/pancreas syndrome: haematological features associated with deletion and duplication of mitochondrial DNAO P Smith, I M Hann, C E Woodward, et al.American Journal of Human Genetics|March 1, 1992
Prenatal diagnosis of mitochondrial DNA8993 T----G diseaseA E Harding, I J Holt, M G Sweeney, et al.Nature Genetics|May 1, 1993
A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathiesM Brockington, M G Sweeney, S R Hammans, et al.American Journal of Human Genetics|October 1, 1992
Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathyM G Sweeney, M B Davis, A Lashwood, et al.Lancet (London, England)|June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samplesS R Hammans, M G Sweeney, M Brockington, et al.The Quarterly Journal of Medicine|July 1, 1993
Mitochondrial DNA transfer RNA mutation Leu(UUR)A-->G 3260: a second family with myopathy and cardiomyopathyM G Sweeney, M Brockington, M J Weston, et al.Journal of the Neurological Sciences|July 1, 1995
Kearns-Sayre syndrome associated with mitochondrial DNA deletion or duplication: a molecular genetic and pathological studyM Brockington, N Alsanjari, M G Sweeney, et al.The Quarterly Journal of Medicine|November 1, 1993
Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) geneM G Sweeney, S Bundey, M Brockington, et al.Pageof 4