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D Devys

Showing results (21-30 of 26) with videos related to

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Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.
Journal of Neurology|January 22, 2008
Hereditary systemic angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy, and hepatopathyD T Winkler, P Lyrer, A Probst, 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.
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.
Journal of Medical Genetics|January 7, 2006
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative studyC Thauvin-Robinet, M Cossée, V Cormier-Daire, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Nature Genetics|May 1, 1995
Cellular localization of the Huntington's disease protein and discrimination of the normal and mutated formY Trottier, D Devys, G Imbert, et al.
Journal of Neurology|January 22, 2008
Hereditary systemic angiopathy (HSA) with cerebral calcifications, retinopathy, progressive nephropathy, and hepatopathyD T Winkler, P Lyrer, A Probst, 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.
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.
Journal of Medical Genetics|January 7, 2006
Clinical, molecular, and genotype-phenotype correlation studies from 25 cases of oral-facial-digital syndrome type 1: a French and Belgian collaborative studyC Thauvin-Robinet, M Cossée, V Cormier-Daire, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
Pageof 3