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Neurogenetics

Showing results (371-380 of 1,080) with videos related to

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Neurogenetics|May 23, 2003
Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the regionDanqing Zhu, Marina Kennerson, John Merory, et al.
Neurogenetics|May 23, 2003
Haplotype analysis of the ETM2 locus in familial essential tremorJoseph J Higgins, Joseph Jankovic, Roni Q Lombardi, et al.
Neurogenetics|May 15, 2012
Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletionsHildegard Kehrer-Sawatzki, Julia Vogt, Tanja Mußotter, et al.
Neurogenetics|May 4, 2012
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesClaudia Dufke, Nina Schlipf, Rebecca Schüle, et al.
Neurogenetics|February 2, 2012
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohortB H Maher, M Kerr, H C Cox, et al.
Neurogenetics|January 25, 2012
Vincristine exacerbates asymptomatic Charcot-Marie-tooth disease with a novel EGR2 mutationTomonori Nakamura, Akihiro Hashiguchi, Shinsuke Suzuki, et al.
Neurogenetics|January 27, 2012
Neuroferritinopathy: a new inborn error of iron metabolismMichael J Keogh, Patricia Jonas, Alan Coulthard, et al.
Neurogenetics|January 6, 2012
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new casesJill A Rosenfeld, Dina Amrom, Eva Andermann, et al.
Neurogenetics|December 30, 2011
New brain-specific beta-synuclein isoforms show expression ratio changes in Lewy body diseasesKatrin Beyer, Ana M Munoz-Marmol, Carolina Sanz, et al.
Neurogenetics|May 1, 1997
The genomic organization of human dystrobrevinH M Sadoulet-Puccio, C A Feener, D J Schaid, et al.
Pageof 108

Showing results (371-380 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|May 23, 2003
Refined localization of dominant intermediate Charcot-Marie-Tooth neuropathy and exclusion of seven known candidate genes in the regionDanqing Zhu, Marina Kennerson, John Merory, et al.
Neurogenetics|May 23, 2003
Haplotype analysis of the ETM2 locus in familial essential tremorJoseph J Higgins, Joseph Jankovic, Roni Q Lombardi, et al.
Neurogenetics|May 15, 2012
Dissecting the clinical phenotype associated with mosaic type-2 NF1 microdeletionsHildegard Kehrer-Sawatzki, Julia Vogt, Tanja Mußotter, et al.
Neurogenetics|May 4, 2012
A high-throughput resequencing microarray for autosomal dominant spastic paraplegia genesClaudia Dufke, Nina Schlipf, Rebecca Schüle, et al.
Neurogenetics|February 2, 2012
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohortB H Maher, M Kerr, H C Cox, et al.
Neurogenetics|January 25, 2012
Vincristine exacerbates asymptomatic Charcot-Marie-tooth disease with a novel EGR2 mutationTomonori Nakamura, Akihiro Hashiguchi, Shinsuke Suzuki, et al.
Neurogenetics|January 27, 2012
Neuroferritinopathy: a new inborn error of iron metabolismMichael J Keogh, Patricia Jonas, Alan Coulthard, et al.
Neurogenetics|January 6, 2012
Genotype-phenotype correlation in interstitial 6q deletions: a report of 12 new casesJill A Rosenfeld, Dina Amrom, Eva Andermann, et al.
Neurogenetics|December 30, 2011
New brain-specific beta-synuclein isoforms show expression ratio changes in Lewy body diseasesKatrin Beyer, Ana M Munoz-Marmol, Carolina Sanz, et al.
Neurogenetics|May 1, 1997
The genomic organization of human dystrobrevinH M Sadoulet-Puccio, C A Feener, D J Schaid, et al.
Pageof 108