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Showing results (51-60 of 70) with videos related to

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Human Molecular Genetics|August 11, 1999
French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysisR P Grewal, G Cancel, E P Leeflang, et al.
Human Genetics|May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 familiesA Lezin, G Cancel, G Stevanin, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Annals of Neurology|December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brainI Gourfinkel-An, G Cancel, Y Trottier, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|June 4, 2017
[Correlation of genetic and cytogenetic alterations in pathological aggressiveness urothelial carcinoma of the bladder: Performance of BCA-1, a mini-array comparative genomic hybridisation-based test]P Léon, G Cancel Tassin, K Sighar, et al.
Nature Genetics|November 1, 1996
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsG Imbert, F Saudou, G Yvert, et al.
Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|October 14, 2015
[Not Available]P Léon, N Kloutidis, J Calves, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, et al.
Pageof 7

Showing results (51-60 of 70) with videos related to

Sort By:
Pageof 7
Human Molecular Genetics|August 11, 1999
French Machado-Joseph disease patients do not exhibit gametic segregation distortion: a sperm typing analysisR P Grewal, G Cancel, E P Leeflang, et al.
Human Genetics|May 1, 1996
Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 familiesA Lezin, G Cancel, G Stevanin, et al.
Annals of Neurology|April 1, 1996
Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological featuresA Dürr, G Stevanin, G Cancel, et al.
Annals of Neurology|December 10, 1997
Differential distribution of the normal and mutated forms of huntingtin in the human brainI Gourfinkel-An, G Cancel, Y Trottier, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|June 4, 2017
[Correlation of genetic and cytogenetic alterations in pathological aggressiveness urothelial carcinoma of the bladder: Performance of BCA-1, a mini-array comparative genomic hybridisation-based test]P Léon, G Cancel Tassin, K Sighar, et al.
Nature Genetics|November 1, 1996
Cloning of the gene for spinocerebellar ataxia 2 reveals a locus with high sensitivity to expanded CAG/glutamine repeatsG Imbert, F Saudou, G Yvert, et al.
Human Molecular Genetics|March 21, 1998
Molecular and clinical correlations in autosomal dominant cerebellar ataxia with progressive macular dystrophy (SCA7)G David, A Dürr, G Stevanin, et al.
Progres En Urologie : Journal De L'Association Francaise D'Urologie Et De La Societe Francaise D'Urologie|October 14, 2015
[Not Available]P Léon, N Kloutidis, J Calves, et al.
Genomics|May 23, 1998
A novel long and unstable CAG/CTG trinucleotide repeat on chromosome 17qT Ikeuchi, K Sanpei, H Takano, et al.
Nature Genetics|September 1, 1997
Cloning of the SCA7 gene reveals a highly unstable CAG repeat expansionG David, N Abbas, G Stevanin, et al.
Pageof 7