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J L Mandel

Showing results (161-170 of 257) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1994
Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994H F Willard, F Cremers, J L Mandel, et al.
Human Molecular Genetics|September 1, 1997
Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathyB M de Gouyon, W Zhao, J Laporte, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Properties of polyglutamine expansion in vitro and in a cellular model for Huntington's diseaseA Lunkes, Y Trottier, J Fagart, et al.
American Journal of Human Genetics|March 1, 1990
The red-green visual pigment gene region in adrenoleukodystrophyP Aubourg, R Feil, S Guidoux, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Polyglutamine expansions and neurodegenerative diseasesF Saudou, D Devys, Y Trottier, et al.
Human Molecular Genetics|October 13, 2000
Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic miceG Yvert, K S Lindenberg, S Picaud, et al.
Human Molecular Genetics|September 16, 1998
Characterization of the myotubularin dual specificity phosphatase gene family from yeast to humanJ Laporte, F Blondeau, A Buj-Bello, et al.
Human Genetics|January 1, 1985
DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosomeM G Mattei, N Philip, E Passage, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Mapping the Friedreich ataxia locus (FRDA) by linkage disequilibrium analysis with highly polymorphic microsatellitesG Sirugo, F Duclos, R Fujita, et al.
Human Genetics|February 1, 1995
De novo missense mutation Y174S in exon 1 of the adrenoleukodystrophy (ALD) geneA Barceló, M Girós, C O Sarde, et al.
Pageof 26

Showing results (161-170 of 257) with videos related to

Sort By:
Pageof 26
Cytogenetics and Cell Genetics|January 1, 1994
Report and abstracts of the Fifth International Workshop on Human X Chromosome Mapping 1994. Heidelberg, Germany, April 24-27, 1994H F Willard, F Cremers, J L Mandel, et al.
Human Molecular Genetics|September 1, 1997
Characterization of mutations in the myotubularin gene in twenty six patients with X-linked myotubular myopathyB M de Gouyon, W Zhao, J Laporte, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 6, 1999
Properties of polyglutamine expansion in vitro and in a cellular model for Huntington's diseaseA Lunkes, Y Trottier, J Fagart, et al.
American Journal of Human Genetics|March 1, 1990
The red-green visual pigment gene region in adrenoleukodystrophyP Aubourg, R Feil, S Guidoux, et al.
Cold Spring Harbor Symposia on Quantitative Biology|January 1, 1996
Polyglutamine expansions and neurodegenerative diseasesF Saudou, D Devys, Y Trottier, et al.
Human Molecular Genetics|October 13, 2000
Expanded polyglutamines induce neurodegeneration and trans-neuronal alterations in cerebellum and retina of SCA7 transgenic miceG Yvert, K S Lindenberg, S Picaud, et al.
Human Molecular Genetics|September 16, 1998
Characterization of the myotubularin dual specificity phosphatase gene family from yeast to humanJ Laporte, F Blondeau, A Buj-Bello, et al.
Human Genetics|January 1, 1985
DNA probe localization at 18p113 band by in situ hybridization and identification of a small supernumerary chromosomeM G Mattei, N Philip, E Passage, et al.
Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie|January 1, 1994
Mapping the Friedreich ataxia locus (FRDA) by linkage disequilibrium analysis with highly polymorphic microsatellitesG Sirugo, F Duclos, R Fujita, et al.
Human Genetics|February 1, 1995
De novo missense mutation Y174S in exon 1 of the adrenoleukodystrophy (ALD) geneA Barceló, M Girós, C O Sarde, et al.
Pageof 26