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J M Vance

Showing results (81-90 of 104) with videos related to

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American Journal of Human Genetics|April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegiaI K Svenson, A E Ashley-Koch, P C Gaskell, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
No association between the APOE gene and autismK L Raiford, Y Shao, I C Allen, et al.
Annals of Human Genetics|October 19, 2006
Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5qS H Shah, W E Kraus, D C Crossman, et al.
Experimental Gerontology|December 13, 2000
Identification of novel genes in late-onset Alzheimer's diseaseM A Pericak-Vance, J Grubber, L R Bailey, et al.
JAMA|October 23, 1997
Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12M A Pericak-Vance, M P Bass, L H Yamaoka, et al.
Neurogenetics|March 25, 2000
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneityM A Pericak-Vance, M C Speer, F Lennon, et al.
Neurogenetics|March 25, 2000
Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegiaW K Scott, P C Gaskell, F Lennon, et al.
Neurogenetics|September 13, 2000
Genetic studies in autistic disorder and chromosome 15M P Bass, M M Menold, C M Wolpert, et al.
Neurogenetics|May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegiaA Ashley-Koch, E R Bonner, P C Gaskell, et al.
Science (New York, N.Y.)|November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophyS Noguchi, E M McNally, K Ben Othmane, et al.
Pageof 11

Showing results (81-90 of 104) with videos related to

Sort By:
Pageof 11
American Journal of Human Genetics|April 20, 2001
Identification and expression analysis of spastin gene mutations in hereditary spastic paraplegiaI K Svenson, A E Ashley-Koch, P C Gaskell, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|February 3, 2004
No association between the APOE gene and autismK L Raiford, Y Shao, I C Allen, et al.
Annals of Human Genetics|October 19, 2006
Serum lipids in the GENECARD study of coronary artery disease identify quantitative trait loci and phenotypic subsets on chromosomes 3q and 5qS H Shah, W E Kraus, D C Crossman, et al.
Experimental Gerontology|December 13, 2000
Identification of novel genes in late-onset Alzheimer's diseaseM A Pericak-Vance, J Grubber, L R Bailey, et al.
JAMA|October 23, 1997
Complete genomic screen in late-onset familial Alzheimer disease. Evidence for a new locus on chromosome 12M A Pericak-Vance, M P Bass, L H Yamaoka, et al.
Neurogenetics|March 25, 2000
Confirmation of a second locus for CMT2 and evidence for additional genetic heterogeneityM A Pericak-Vance, M C Speer, F Lennon, et al.
Neurogenetics|March 25, 2000
Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegiaW K Scott, P C Gaskell, F Lennon, et al.
Neurogenetics|September 13, 2000
Genetic studies in autistic disorder and chromosome 15M P Bass, M M Menold, C M Wolpert, et al.
Neurogenetics|May 17, 2001
Fine mapping and genetic heterogeneity in the pure form of autosomal dominant familial spastic paraplegiaA Ashley-Koch, E R Bonner, P C Gaskell, et al.
Science (New York, N.Y.)|November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophyS Noguchi, E M McNally, K Ben Othmane, et al.
Pageof 11