Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

M G Sweeney

Showing results (1-10 of 48) with videos related to

Pageof 5
Sort By:
Lancet (London, England)|January 6, 2001
Increased risk of stroke in patients with the A12308G polymorphism in mitochondriaT Pulkes, M G Sweeney, M G Hanna
Brain : a Journal of Neurology|October 1, 1995
Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of WalworthP Giunti, M G Sweeney, A E Harding
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 23, 2003
Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplicationW Marques, M G Sweeney, N W Wood
American Journal of Human Genetics|July 1, 1995
Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutationA E Harding, M G Sweeney, G G Govan, et al.
Archives of Disease in Childhood|November 1, 1994
Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'A Fryer, R Appleton, M G Sweeney, et al.
Annals of Neurology|May 19, 1998
Dejerine-Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible "hot spot" on Ser72W Marques, P K Thomas, M G Sweeney, 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.
Journal of Neurology|April 1, 1997
Mitochondrial DNA polymorphisms in pathologically proven Parkinson's diseaseO Bandmann, M G Sweeney, S E Daniel, 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.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Lancet (London, England)|January 6, 2001
Increased risk of stroke in patients with the A12308G polymorphism in mitochondriaT Pulkes, M G Sweeney, M G Hanna
Brain : a Journal of Neurology|October 1, 1995
Detection of the Machado-Joseph disease/spinocerebellar ataxia three trinucleotide repeat expansion in families with autosomal dominant motor disorders, including the Drew family of WalworthP Giunti, M G Sweeney, A E Harding
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|September 23, 2003
Thr(118)Met amino acid substitution in the peripheral myelin protein 22 does not influence the clinical phenotype of Charcot-Marie-Tooth disease type 1A due to the 17p11.2-p12 duplicationW Marques, M G Sweeney, N W Wood
American Journal of Human Genetics|July 1, 1995
Pedigree analysis in Leber hereditary optic neuropathy families with a pathogenic mtDNA mutationA E Harding, M G Sweeney, G G Govan, et al.
Archives of Disease in Childhood|November 1, 1994
Mitochondrial DNA 8993 (NARP) mutation presenting with a heterogeneous phenotype including 'cerebral palsy'A Fryer, R Appleton, M G Sweeney, et al.
Annals of Neurology|May 19, 1998
Dejerine-Sottas neuropathy and PMP22 point mutations: a new base pair substitution and a possible "hot spot" on Ser72W Marques, P K Thomas, M G Sweeney, 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.
Journal of Neurology|April 1, 1997
Mitochondrial DNA polymorphisms in pathologically proven Parkinson's diseaseO Bandmann, M G Sweeney, S E Daniel, 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.
Pageof 5