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Neurogenetics

Showing results (751-760 of 949) with videos related to

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Neurogenetics|March 29, 2000
Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patientsM Vorgerd, B Burwinkel, H Reichmann, et al.
Neurogenetics|March 29, 2000
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosisT Siddique, M A Pericak-Vance, J Caliendo, et al.
Neurogenetics|March 25, 2000
Isolation and characterization of trinucleotide repeat containing partial transcripts in human spinal cordN Kaushik, A Malaspina, M Schalling, et al.
Neurogenetics|March 25, 2000
Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) geneJ R Gilbert, V Guy, A Kumar, et al.
Neurogenetics|March 25, 2000
Identification of a novel missense mutation of the SMN(T) gene in two siblings with spinal muscular atrophyC H Wang, B D Papendick, P Bruinsma, et al.
Neurogenetics|March 25, 2000
The Y-chromosomal genes SRY and ZFY are transcribed in adult human brainA Mayer, G Lahr, D F Swaab, 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|March 25, 2000
Emerin, deficiency of which causes Emery-Dreifuss muscular dystrophy, is localized at the inner nuclear membraneH Yorifuji, Y Tadano, Y Tsuchiya, et al.
Neurogenetics|September 13, 2000
Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)M G Spillantini, J C Van Swieten, M Goedert
Neurogenetics|May 1, 1997
A model for susceptibility polymorphisms for complex diseases: apolipoprotein E and Alzheimer diseaseA D Roses
Pageof 95

Showing results (751-760 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|March 29, 2000
Adult-onset glycogen storage disease type II: phenotypic and allelic heterogeneity in German patientsM Vorgerd, B Burwinkel, H Reichmann, et al.
Neurogenetics|March 29, 2000
Lack of association between apolipoprotein E genotype and sporadic amyotrophic lateral sclerosisT Siddique, M A Pericak-Vance, J Caliendo, et al.
Neurogenetics|March 25, 2000
Isolation and characterization of trinucleotide repeat containing partial transcripts in human spinal cordN Kaushik, A Malaspina, M Schalling, et al.
Neurogenetics|March 25, 2000
Mutation and polymorphism analysis in the tuberous sclerosis 2 (TSC2) geneJ R Gilbert, V Guy, A Kumar, et al.
Neurogenetics|March 25, 2000
Identification of a novel missense mutation of the SMN(T) gene in two siblings with spinal muscular atrophyC H Wang, B D Papendick, P Bruinsma, et al.
Neurogenetics|March 25, 2000
The Y-chromosomal genes SRY and ZFY are transcribed in adult human brainA Mayer, G Lahr, D F Swaab, 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|March 25, 2000
Emerin, deficiency of which causes Emery-Dreifuss muscular dystrophy, is localized at the inner nuclear membraneH Yorifuji, Y Tadano, Y Tsuchiya, et al.
Neurogenetics|September 13, 2000
Tau gene mutations in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)M G Spillantini, J C Van Swieten, M Goedert
Neurogenetics|May 1, 1997
A model for susceptibility polymorphisms for complex diseases: apolipoprotein E and Alzheimer diseaseA D Roses
Pageof 95