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P F Chinnery

Showing results (21-30 of 152) with videos related to

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Neuromuscular Disorders : NMD|May 11, 2006
Is selection required for the accumulation of somatic mitochondrial DNA mutations in post-mitotic cells?S E Durham, D C Samuels, P F Chinnery
Journal of Medical Genetics|March 19, 2002
Leber hereditary optic neuropathyP Yu-Wai-Man, D M Turnbull, P F Chinnery
Journal of Medical Genetics|August 27, 1998
Mitochondrial DNA mutations and pathogenicityP F Chinnery, D M Turnbull, N Howell, et al.
Journal of the Neurological Sciences|May 28, 2003
Clinical progression of mitochondrial myopathy is associated with the random accumulation of cytochrome c oxidase negative skeletal muscle fibresP F Chinnery, D Howel, D M Turnbull, et al.
Neurology|September 9, 2011
Recurrent stroke-like episodes in X-linked Charcot-Marie-Tooth diseaseA Basu, R Horvath, B Esisi, et al.
Neurology|January 26, 2005
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicismG Hudson, M Deschauer, K Busse, et al.
American Journal of Human Genetics|December 5, 1998
Genetic counseling and prenatal diagnosis for mtDNA diseaseP F Chinnery, N Howell, R N Lightowlers, et al.
Journal of Medical Genetics|July 29, 1999
Mitochondrial DNA analysis: polymorphisms and pathogenicityP F Chinnery, N Howell, R M Andrews, et al.
Journal of Medical Genetics|June 30, 2000
Clinical mitochondrial geneticsP F Chinnery, N Howell, R M Andrews, et al.
Brain : a Journal of Neurology|November 20, 1997
Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypesP F Chinnery, N Howell, R N Lightowlers, et al.
Pageof 16

Showing results (21-30 of 152) with videos related to

Sort By:
Pageof 16
Neuromuscular Disorders : NMD|May 11, 2006
Is selection required for the accumulation of somatic mitochondrial DNA mutations in post-mitotic cells?S E Durham, D C Samuels, P F Chinnery
Journal of Medical Genetics|March 19, 2002
Leber hereditary optic neuropathyP Yu-Wai-Man, D M Turnbull, P F Chinnery
Journal of Medical Genetics|August 27, 1998
Mitochondrial DNA mutations and pathogenicityP F Chinnery, D M Turnbull, N Howell, et al.
Journal of the Neurological Sciences|May 28, 2003
Clinical progression of mitochondrial myopathy is associated with the random accumulation of cytochrome c oxidase negative skeletal muscle fibresP F Chinnery, D Howel, D M Turnbull, et al.
Neurology|September 9, 2011
Recurrent stroke-like episodes in X-linked Charcot-Marie-Tooth diseaseA Basu, R Horvath, B Esisi, et al.
Neurology|January 26, 2005
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicismG Hudson, M Deschauer, K Busse, et al.
American Journal of Human Genetics|December 5, 1998
Genetic counseling and prenatal diagnosis for mtDNA diseaseP F Chinnery, N Howell, R N Lightowlers, et al.
Journal of Medical Genetics|July 29, 1999
Mitochondrial DNA analysis: polymorphisms and pathogenicityP F Chinnery, N Howell, R M Andrews, et al.
Journal of Medical Genetics|June 30, 2000
Clinical mitochondrial geneticsP F Chinnery, N Howell, R M Andrews, et al.
Brain : a Journal of Neurology|November 20, 1997
Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypesP F Chinnery, N Howell, R N Lightowlers, et al.
Pageof 16