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American Journal of Human Genetics
|
July 1, 1996
Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy
R M Chalmers, M B Davis, M G Sweeney, 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 cardiomyopathy
M G Sweeney, M Brockington, M J Weston, et al.
Lancet (London, England)
|
June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples
S R Hammans, M G Sweeney, M Brockington, et al.
Brain : a Journal of Neurology
|
April 1, 1992
A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies
S R Hammans, M G Sweeney, D A Wicks, 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 study
M 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) gene
M G Sweeney, S Bundey, M Brockington, et al.
Journal of Neurology
|
August 27, 1999
Phenotypic variation of a new P0 mutation in genetically identical twins
W Marques, M G Hanna, S R Marques, et al.
Journal of Neurology
|
February 3, 2012
Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion
G Koutsis, G Karadima, A Pandraud, et al.
Brain : a Journal of Neurology
|
August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
P Giunti, M G Sweeney, M Spadaro, et al.
Brain : a Journal of Neurology
|
June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study
S R Hammans, M G Sweeney, M G Hanna, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
American Journal of Human Genetics
|
July 1, 1996
Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathy
R M Chalmers, M B Davis, M G Sweeney, 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 cardiomyopathy
M G Sweeney, M Brockington, M J Weston, et al.
Lancet (London, England)
|
June 1, 1991
Mitochondrial encephalopathies: molecular genetic diagnosis from blood samples
S R Hammans, M G Sweeney, M Brockington, et al.
Brain : a Journal of Neurology
|
April 1, 1992
A molecular genetic study of focal histochemical defects in mitochondrial encephalomyopathies
S R Hammans, M G Sweeney, D A Wicks, 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 study
M 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) gene
M G Sweeney, S Bundey, M Brockington, et al.
Journal of Neurology
|
August 27, 1999
Phenotypic variation of a new P0 mutation in genetically identical twins
W Marques, M G Hanna, S R Marques, et al.
Journal of Neurology
|
February 3, 2012
Genetic screening of Greek patients with Huntington’s disease phenocopies identifies an SCA8 expansion
G Koutsis, G Karadima, A Pandraud, et al.
Brain : a Journal of Neurology
|
August 1, 1994
The trinucleotide repeat expansion on chromosome 6p (SCA1) in autosomal dominant cerebellar ataxias
P Giunti, M G Sweeney, M Spadaro, et al.
Brain : a Journal of Neurology
|
June 1, 1995
The mitochondrial DNA transfer RNALeu(UUR) A-->G(3243) mutation. A clinical and genetic study
S R Hammans, M G Sweeney, M G Hanna, et al.
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of 5