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Neurology
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February 1, 1997
Longitudinal change in basal ganglia volume in patients with Huntington's disease
E H Aylward, Q Li, O C Stine, et al.
Cancer Research
|
August 17, 2001
Instabilotyping: comprehensive identification of frameshift mutations caused by coding region microsatellite instability
Y Mori, J Yin, A Rashid, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 1, 2000
Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease
E H Aylward, A M Codori, A Rosenblatt, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Adrenoleukodystrophy: phenotypic variability and implications for therapy
H W Moser, A B Moser, K D Smith, et al.
Brain Research. Molecular Brain Research
|
March 1, 1996
DRPLA gene (atrophin-1) sequence and mRNA expression in human brain
R L Margolis, S H Li, W S Young, et al.
Journal of Medical Genetics
|
February 9, 1999
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expression
R L Margolis, O C Stine, C M Ward, et al.
American Journal of Human Genetics
|
September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease
N G Ranen, O C Stine, M H Abbott, et al.
Pediatric Research
|
November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observations
O Hurko, D R Johns, S L Rutledge, et al.
Human Genetics
|
July 1, 1997
cDNAs with long CAG trinucleotide repeats from human brain
R L Margolis, M R Abraham, S B Gatchell, et al.
Neuron
|
November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissues
S H Li, G Schilling, W S Young, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 69) with videos related to
Sort By:
Page
of 7
Neurology
|
February 1, 1997
Longitudinal change in basal ganglia volume in patients with Huntington's disease
E H Aylward, Q Li, O C Stine, et al.
Cancer Research
|
August 17, 2001
Instabilotyping: comprehensive identification of frameshift mutations caused by coding region microsatellite instability
Y Mori, J Yin, A Rashid, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
June 1, 2000
Rate of caudate atrophy in presymptomatic and symptomatic stages of Huntington's disease
E H Aylward, A M Codori, A Rosenblatt, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1992
Adrenoleukodystrophy: phenotypic variability and implications for therapy
H W Moser, A B Moser, K D Smith, et al.
Brain Research. Molecular Brain Research
|
March 1, 1996
DRPLA gene (atrophin-1) sequence and mRNA expression in human brain
R L Margolis, S H Li, W S Young, et al.
Journal of Medical Genetics
|
February 9, 1999
Unstable expansion of the CAG trinucleotide repeat in MAB21L1: report of a second pedigree and effect on protein expression
R L Margolis, O C Stine, C M Ward, et al.
American Journal of Human Genetics
|
September 1, 1995
Anticipation and instability of IT-15 (CAG)n repeats in parent-offspring pairs with Huntington disease
N G Ranen, O C Stine, M H Abbott, et al.
Pediatric Research
|
November 1, 1990
Heteroplasmy in chronic external ophthalmoplegia: clinical and molecular observations
O Hurko, D R Johns, S L Rutledge, et al.
Human Genetics
|
July 1, 1997
cDNAs with long CAG trinucleotide repeats from human brain
R L Margolis, M R Abraham, S B Gatchell, et al.
Neuron
|
November 1, 1993
Huntington's disease gene (IT15) is widely expressed in human and rat tissues
S H Li, G Schilling, W S Young, et al.
Page
of 7