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Neurogenetics

Showing results (291-300 of 1,080) with videos related to

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Neurogenetics|June 22, 2020
Novel familial IQSEC2 pathogenic sequence variant associated with neurodevelopmental disorders and epilepsyMarketa Wayhelova, Michal Ryzí, Jan Oppelt, et al.
Neurogenetics|January 20, 2005
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosisYi-Ju Li, Margaret A Pericak-Vance, Jonathan L Haines, et al.
Neurogenetics|July 9, 2004
Heterozygous mutation in 5'-untranslated region of sepiapterin reductase gene (SPR) in a patient with dopa-responsive dystoniaDaniela Steinberger, Nenad Blau, Dimitri Goriuonov, et al.
Neurogenetics|July 9, 2004
Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genesCindy Kok, Marina L Kennerson, Simon J Myers, et al.
Neurogenetics|October 19, 2004
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphismP Saccucci, M Verdecchia, A Piciullo, et al.
Neurogenetics|October 19, 2004
Dementia with Lewy bodies: no association of polymorphisms in the human synphilin geneJ Busby, K K O'Brien, A M Gibson, et al.
Neurogenetics|April 15, 2005
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraineR A Lea, D R Nyholt, R P Curtain, et al.
Neurogenetics|April 17, 2004
Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer diseaseMia E-L Blomqvist, Peter A Silburn, Daniel D Buchanan, et al.
Neurogenetics|January 19, 2005
MLPA analysis for the detection of deletions, duplications and complex rearrangements in the dystrophin gene: potential and pitfallsB Janssen, C Hartmann, V Scholz, et al.
Neurogenetics|January 1, 2005
PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2Ken Inoue
Pageof 108

Showing results (291-300 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|June 22, 2020
Novel familial IQSEC2 pathogenic sequence variant associated with neurodevelopmental disorders and epilepsyMarketa Wayhelova, Michal Ryzí, Jan Oppelt, et al.
Neurogenetics|January 20, 2005
Apolipoprotein E is associated with age at onset of amyotrophic lateral sclerosisYi-Ju Li, Margaret A Pericak-Vance, Jonathan L Haines, et al.
Neurogenetics|July 9, 2004
Heterozygous mutation in 5'-untranslated region of sepiapterin reductase gene (SPR) in a patient with dopa-responsive dystoniaDaniela Steinberger, Nenad Blau, Dimitri Goriuonov, et al.
Neurogenetics|July 9, 2004
Transcript map of the candidate region for HSNI with cough and gastroesophageal reflux on chromosome 3p and exclusion of candidate genesCindy Kok, Marina L Kennerson, Simon J Myers, et al.
Neurogenetics|October 19, 2004
Convulsive disorder and genetic polymorphism. Association of idiopathic generalized epilepsy with haptoglobin polymorphismP Saccucci, M Verdecchia, A Piciullo, et al.
Neurogenetics|October 19, 2004
Dementia with Lewy bodies: no association of polymorphisms in the human synphilin geneJ Busby, K K O'Brien, A M Gibson, et al.
Neurogenetics|April 15, 2005
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraineR A Lea, D R Nyholt, R P Curtain, et al.
Neurogenetics|April 17, 2004
Sequence variation in the proximity of IDE may impact age at onset of both Parkinson disease and Alzheimer diseaseMia E-L Blomqvist, Peter A Silburn, Daniel D Buchanan, et al.
Neurogenetics|January 19, 2005
MLPA analysis for the detection of deletions, duplications and complex rearrangements in the dystrophin gene: potential and pitfallsB Janssen, C Hartmann, V Scholz, et al.
Neurogenetics|January 1, 2005
PLP1-related inherited dysmyelinating disorders: Pelizaeus-Merzbacher disease and spastic paraplegia type 2Ken Inoue
Pageof 108