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Clinical Genetics
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May 15, 2009
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity
A Boukhris, G Stevanin, I Feki, et al.
Brain : a Journal of Neurology
|
September 26, 2001
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia
H Fujigasaki, J J Martin, P P De Deyn, et al.
Neurology
|
June 15, 2007
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
P Charles, A Camuzat, N Benammar, et al.
American Journal of Human Genetics
|
May 23, 2000
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation
A Herman-Bert, G Stevanin, J C Netter, et al.
European Journal of Neurology
|
July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormality
N Collongues, C Depienne, N Boehm, et al.
Molecular Medicine (Cambridge, Mass.)
|
January 1, 1996
Mutation detection in Machado-Joseph disease using repeat expansion detection
K Lindblad, A Lunkes, P Maciel, et al.
Neurology
|
March 17, 1999
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families
M Dichgans, L Schöls, J Herzog, et al.
Human Molecular Genetics
|
August 11, 1999
French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysis
R P Grewal, G Cancel, E P Leeflang, et al.
Neurology
|
March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients
G Stevanin, A Camuzat, S E Holmes, et al.
Human Genetics
|
May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families
A Lezin, G Cancel, G Stevanin, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 81) with videos related to
Sort By:
Page
of 9
Clinical Genetics
|
May 15, 2009
Tunisian hereditary spastic paraplegias: clinical variability supported by genetic heterogeneity
A Boukhris, G Stevanin, I Feki, et al.
Brain : a Journal of Neurology
|
September 26, 2001
CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia
H Fujigasaki, J J Martin, P P De Deyn, et al.
Neurology
|
June 15, 2007
Are interrupted SCA2 CAG repeat expansions responsible for parkinsonism?
P Charles, A Camuzat, N Benammar, et al.
American Journal of Human Genetics
|
May 23, 2000
Mapping of spinocerebellar ataxia 13 to chromosome 19q13.3-q13.4 in a family with autosomal dominant cerebellar ataxia and mental retardation
A Herman-Bert, G Stevanin, J C Netter, et al.
European Journal of Neurology
|
July 14, 2012
Novel SPG10 mutation associated with dysautonomia, spinal cord atrophy, and skin biopsy abnormality
N Collongues, C Depienne, N Boehm, et al.
Molecular Medicine (Cambridge, Mass.)
|
January 1, 1996
Mutation detection in Machado-Joseph disease using repeat expansion detection
K Lindblad, A Lunkes, P Maciel, et al.
Neurology
|
March 17, 1999
Spinocerebellar ataxia type 6: evidence for a strong founder effect among German families
M Dichgans, L Schöls, J Herzog, et al.
Human Molecular Genetics
|
August 11, 1999
French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysis
R P Grewal, G Cancel, E P Leeflang, et al.
Neurology
|
March 27, 2002
CAG/CTG repeat expansions at the Huntington's disease-like 2 locus are rare in Huntington's disease patients
G Stevanin, A Camuzat, S E Holmes, et al.
Human Genetics
|
May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families
A Lezin, G Cancel, G Stevanin, et al.
Page
of 9