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G Stevanin

Showing results (21-30 of 81) with videos related to

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American Journal of Medical Genetics|October 9, 1995
SCA2 is not a major locus for ADCA type I in French familiesG Cancel, G Stevanin, A Dürr, et al.
Human Molecular Genetics|September 1, 1993
Genetic heterogeneity of autosomal dominant cerebellar ataxia type I: evidence for the existence of a third locusG Stevanin, H Chneiweiss, E Le Guern, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
Clinical and genetic study of familial essential tremor in an isolate of Northern TajikistanS N Illarioshkin, I A Ivanova-Smolenskaya, R A Rahmonov, et al.
Human Mutation|February 5, 1998
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph diseaseG Cancel, I Gourfinkel-An, G Stevanin, et al.
American Journal of Human Genetics|November 1, 1995
Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutationG Stevanin, G Cancel, O Didierjean, et al.
Neurology|June 1, 1993
Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French familiesC Khati, G Stevanin, A Durr, et al.
Annals of Neurology|April 1, 1994
Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type IA Benomar, E Le Guern, A Dürr, et al.
Nature Genetics|January 1, 1994
Is DRPLA also linked to 14q?G Cancel, A Dürr, G Stevanin, et al.
Journal of Medical Genetics|October 1, 1995
Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph diseaseG Stevanin, E Cassa, G Cancel, et al.
American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.
Pageof 9

Showing results (21-30 of 81) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|October 9, 1995
SCA2 is not a major locus for ADCA type I in French familiesG Cancel, G Stevanin, A Dürr, et al.
Human Molecular Genetics|September 1, 1993
Genetic heterogeneity of autosomal dominant cerebellar ataxia type I: evidence for the existence of a third locusG Stevanin, H Chneiweiss, E Le Guern, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 29, 2000
Clinical and genetic study of familial essential tremor in an isolate of Northern TajikistanS N Illarioshkin, I A Ivanova-Smolenskaya, R A Rahmonov, et al.
Human Mutation|February 5, 1998
Somatic mosaicism of the CAG repeat expansion in spinocerebellar ataxia type 3/Machado-Joseph diseaseG Cancel, I Gourfinkel-An, G Stevanin, et al.
American Journal of Human Genetics|November 1, 1995
Linkage disequilibrium at the Machado-Joseph disease/spinal cerebellar ataxia 3 locus: evidence for a common founder effect in French and Portuguese-Brazilian families as well as a second ancestral Portuguese-Azorean mutationG Stevanin, G Cancel, O Didierjean, et al.
Neurology|June 1, 1993
Genetic heterogeneity of autosomal dominant cerebellar ataxia type 1: clinical and genetic analysis of 10 French familiesC Khati, G Stevanin, A Durr, et al.
Annals of Neurology|April 1, 1994
Autosomal-dominant cerebellar ataxia with retinal degeneration (ADCA type II) is genetically different from ADCA type IA Benomar, E Le Guern, A Dürr, et al.
Nature Genetics|January 1, 1994
Is DRPLA also linked to 14q?G Cancel, A Dürr, G Stevanin, et al.
Journal of Medical Genetics|October 1, 1995
Characterisation of the unstable expanded CAG repeat in the MJD1 gene in four Brazilian families of Portuguese descent with Machado-Joseph diseaseG Stevanin, E Cassa, G Cancel, et al.
American Journal of Human Genetics|January 1, 1995
The gene for spinal cerebellar ataxia 3 (SCA3) is located in a region of approximately 3 cM on chromosome 14q24.3-q32.2G Stevanin, G Cancel, A Dürr, et al.
Pageof 9