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Wendy M Hutchison

Showing results (1-10 of 4) with videos related to

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Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2007
Levodopa response in Parkinsonism with multiple mitochondrial DNA deletionsRobert A Wilcox, Andrew Churchyard, Henrik H Dahl, et al.
The Journal of Molecular Diagnostics : JMD|August 26, 2006
Detection of mutations in genes associated with hearing loss using a microarray-based approachKirby Siemering, Shehnaaz S M Manji, Wendy M Hutchison, et al.
Archives of Neurology|December 14, 2005
Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) geneWendy M Hutchison, Dominic Thyagarajan, Joanna Poulton, et al.
American Journal of Human Genetics|October 23, 2008
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial diseaseCanny Sugiana, David J Pagliarini, Matthew McKenzie, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Movement Disorders : Official Journal of the Movement Disorder Society|March 16, 2007
Levodopa response in Parkinsonism with multiple mitochondrial DNA deletionsRobert A Wilcox, Andrew Churchyard, Henrik H Dahl, et al.
The Journal of Molecular Diagnostics : JMD|August 26, 2006
Detection of mutations in genes associated with hearing loss using a microarray-based approachKirby Siemering, Shehnaaz S M Manji, Wendy M Hutchison, et al.
Archives of Neurology|December 14, 2005
Clinical and molecular features of encephalomyopathy due to the A3302G mutation in the mitochondrial tRNA(Leu(UUR)) geneWendy M Hutchison, Dominic Thyagarajan, Joanna Poulton, et al.
American Journal of Human Genetics|October 23, 2008
Mutation of C20orf7 disrupts complex I assembly and causes lethal neonatal mitochondrial diseaseCanny Sugiana, David J Pagliarini, Matthew McKenzie, et al.
Pageof 1