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Neurogenetics

Showing results (641-650 of 949) with videos related to

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Neurogenetics|October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)C D Coldren, Z Lai, P Shragg, et al.
Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
Neurogenetics|November 4, 2010
The effect of SNCA 3' region on the levels of SNCA-112 splicing variantJeanette J McCarthy, Colton Linnertz, Laura Saucier, et al.
Neurogenetics|April 3, 2013
The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonismsAntonino Cannas, Giuseppe Borghero, Gian Luca Floris, et al.
Neurogenetics|February 5, 2013
Natural history of neurofibromatosis type 2 with onset before the age of 1 yearMartino Ruggieri, Anna Lia Gabriele, Agata Polizzi, et al.
Neurogenetics|May 7, 2013
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onsetEliana Marisa Ramos, Jeanne C Latourelle, Tammy Gillis, et al.
Neurogenetics|November 21, 2013
PIGN mutations cause congenital anomalies, developmental delay, hypotonia, epilepsy, and progressive cerebellar atrophyChihiro Ohba, Nobuhiko Okamoto, Yoshiko Murakami, et al.
Neurogenetics|October 9, 2013
Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndromeAxel Weber, Angelika Köhler, Andreas Hahn, et al.
Neurogenetics|October 5, 2013
Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhoodChihiro Ohba, Hitoshi Osaka, Mizue Iai, et al.
Neurogenetics|August 22, 2014
Genes and gene networks implicated in aggression related behaviourKarim Malki, Oliver Pain, Ebba Du Rietz, et al.
Pageof 95

Showing results (641-650 of 949) with videos related to

Sort By:
Pageof 95
Neurogenetics|October 16, 2008
Chromosomal microarray mapping suggests a role for BSX and Neurogranin in neurocognitive and behavioral defects in the 11q terminal deletion disorder (Jacobsen syndrome)C D Coldren, Z Lai, P Shragg, et al.
Neurogenetics|January 10, 2009
A systematic comparison of all mutations in hereditary sensory neuropathy type I (HSAN I) reveals that the G387A mutation is not disease associatedThorsten Hornemann, Anke Penno, Stephane Richard, et al.
Neurogenetics|November 4, 2010
The effect of SNCA 3' region on the levels of SNCA-112 splicing variantJeanette J McCarthy, Colton Linnertz, Laura Saucier, et al.
Neurogenetics|April 3, 2013
The p.A382T TARDBP gene mutation in Sardinian patients affected by Parkinson's disease and other degenerative parkinsonismsAntonino Cannas, Giuseppe Borghero, Gian Luca Floris, et al.
Neurogenetics|February 5, 2013
Natural history of neurofibromatosis type 2 with onset before the age of 1 yearMartino Ruggieri, Anna Lia Gabriele, Agata Polizzi, et al.
Neurogenetics|May 7, 2013
Candidate glutamatergic and dopaminergic pathway gene variants do not influence Huntington's disease motor onsetEliana Marisa Ramos, Jeanne C Latourelle, Tammy Gillis, et al.
Neurogenetics|November 21, 2013
PIGN mutations cause congenital anomalies, developmental delay, hypotonia, epilepsy, and progressive cerebellar atrophyChihiro Ohba, Nobuhiko Okamoto, Yoshiko Murakami, et al.
Neurogenetics|October 9, 2013
Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndromeAxel Weber, Angelika Köhler, Andreas Hahn, et al.
Neurogenetics|October 5, 2013
Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhoodChihiro Ohba, Hitoshi Osaka, Mizue Iai, et al.
Neurogenetics|August 22, 2014
Genes and gene networks implicated in aggression related behaviourKarim Malki, Oliver Pain, Ebba Du Rietz, et al.
Pageof 95