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A Lunkes

Showing results (11-20 of 17) with videos related to

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Genomics|September 1, 1993
Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2)I Silveira, A Manaia, J Melki, et al.
American Journal of Human Genetics|October 1, 1995
Localization of the candidate gene D-amino acid oxidase outside the refined I-cM region of spinocerebellar ataxia 2S Gispert, A Lunkes, N Santos, et al.
Molecular Medicine (Cambridge, Mass.)|January 1, 1996
Mutation detection in Machado-Joseph disease using repeat expansion detectionK Lindblad, A Lunkes, P Maciel, et al.
Annals of Neurology|April 1, 1996
Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1L G Goldfarb, O Vasconcelos, F A Platonov, et al.
Genomics|January 1, 1996
A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197G Auburger, T Ratzlaff, A Lunkes, et al.
Nature Genetics|November 1, 1996
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2S M Pulst, A Nechiporuk, T Nechiporuk, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Genomics|September 1, 1993
Machado-Joseph disease is genetically different from Holguin dominant ataxia (SCA2)I Silveira, A Manaia, J Melki, et al.
American Journal of Human Genetics|October 1, 1995
Localization of the candidate gene D-amino acid oxidase outside the refined I-cM region of spinocerebellar ataxia 2S Gispert, A Lunkes, N Santos, et al.
Molecular Medicine (Cambridge, Mass.)|January 1, 1996
Mutation detection in Machado-Joseph disease using repeat expansion detectionK Lindblad, A Lunkes, P Maciel, et al.
Annals of Neurology|April 1, 1996
Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1L G Goldfarb, O Vasconcelos, F A Platonov, et al.
Genomics|January 1, 1996
A gene for autosomal dominant paroxysmal choreoathetosis/spasticity (CSE) maps to the vicinity of a potassium channel gene cluster on chromosome 1p, probably within 2 cM between D1S443 and D1S197G Auburger, T Ratzlaff, A Lunkes, et al.
Nature Genetics|November 1, 1996
Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2S M Pulst, A Nechiporuk, T Nechiporuk, et al.
Neurogenetics|May 1, 1997
SCA2 trinucleotide expansion in German SCA patientsO Riess, F A Laccone, S Gispert, et al.
Pageof 2