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H R Horvitz

Showing results (161-170 of 169) with videos related to

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Human Molecular Genetics|November 1, 1992
Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1)D H Donaldson, D R Rosen, J O'Regan, et al.
Human Molecular Genetics|October 1, 1992
Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1D R Rosen, P C Sapp, J O'Regan, et al.
Human Genetics|November 1, 1994
Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21P Gregor, S M Gaston, X Yang, et al.
Annals of Neurology|February 1, 1997
Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosisM E Cudkowicz, D McKenna-Yasek, P E Sapp, et al.
Neurogenetics|May 18, 1999
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33B A Hosler, P C Sapp, R Berger, et al.
Neurology|January 20, 2006
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementiaM Morita, A Al-Chalabi, P M Andersen, et al.
JAMA|October 4, 2000
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22B A Hosler, T Siddique, P C Sapp, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosisB A Hosler, G A Nicholson, P C Sapp, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Pageof 17

Showing results (161-170 of 169) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 169 results.
Human Molecular Genetics|November 1, 1992
Two independent dinucleotide repeat polymorphisms at the D21S235 locus (21q22.1)D H Donaldson, D R Rosen, J O'Regan, et al.
Human Molecular Genetics|October 1, 1992
Dinucleotide repeat polymorphisms (D21S223 and D21S224) at 21q22.1D R Rosen, P C Sapp, J O'Regan, et al.
Human Genetics|November 1, 1994
Genetic and physical mapping of the GLUR5 glutamate receptor gene on human chromosome 21P Gregor, S M Gaston, X Yang, et al.
Annals of Neurology|February 1, 1997
Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosisM E Cudkowicz, D McKenna-Yasek, P E Sapp, et al.
Neurogenetics|May 18, 1999
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33B A Hosler, P C Sapp, R Berger, et al.
Neurology|January 20, 2006
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementiaM Morita, A Al-Chalabi, P M Andersen, et al.
JAMA|October 4, 2000
Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22B A Hosler, T Siddique, P C Sapp, et al.
Neuromuscular Disorders : NMD|October 1, 1996
Three novel mutations and two variants in the gene for Cu/Zn superoxide dismutase in familial amyotrophic lateral sclerosisB A Hosler, G A Nicholson, P C Sapp, et al.
Science (New York, N.Y.)|March 3, 2009
Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosisT J Kwiatkowski, D A Bosco, A L Leclerc, et al.
Pageof 17