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Neurogenetics

Showing results (351-360 of 1,080) with videos related to

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Neurogenetics|June 22, 2018
Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findingsR C Caylor, L Grote, I Thiffault, et al.
Neurogenetics|November 18, 2003
Mutation analysis of CBL-C and SPRED3 on 19q in human glioblastomaMasahiro Mizoguchi, Catherine L Nutt, David N Louis
Neurogenetics|September 25, 2003
Genotypic association of exonic LGI4 polymorphisms and childhood absence epilepsyWenli Gu, Thomas Sander, Tim Becker, et al.
Neurogenetics|December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locusM Muglia, C Criscuolo, A Magariello, et al.
Neurogenetics|October 18, 2007
Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer's diseaseJoseph H Lee, Sandra Barral, Rong Cheng, et al.
Neurogenetics|November 10, 2007
Refinement of the 2p11.1-q12.2 locus responsible for cortical tremor associated with epilepsy and exclusion of candidate genesCécile Saint-Martin, Delphine Bouteiller, Giovanni Stevanin, et al.
Neurogenetics|August 9, 2008
A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22-q13.12E Chouery, J Kfoury, V Delague, et al.
Neurogenetics|October 14, 2008
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosisE Stogmann, S El Tawil, J Wagenstaller, et al.
Neurogenetics|July 30, 2008
Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2)Larissa Arning, Ludger Schöls, Huriye Cin, et al.
Neurogenetics|June 20, 2008
Heterogeneous dysregulation of microRNAs across the autism spectrumKawther Abu-Elneel, Tsunglin Liu, Francesca S Gazzaniga, et al.
Pageof 108

Showing results (351-360 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|June 22, 2018
Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findingsR C Caylor, L Grote, I Thiffault, et al.
Neurogenetics|November 18, 2003
Mutation analysis of CBL-C and SPRED3 on 19q in human glioblastomaMasahiro Mizoguchi, Catherine L Nutt, David N Louis
Neurogenetics|September 25, 2003
Genotypic association of exonic LGI4 polymorphisms and childhood absence epilepsyWenli Gu, Thomas Sander, Tim Becker, et al.
Neurogenetics|December 6, 2003
Narrowing of the critical region in autosomal recessive spastic paraplegia linked to the SPG5 locusM Muglia, C Criscuolo, A Magariello, et al.
Neurogenetics|October 18, 2007
Age-at-onset linkage analysis in Caribbean Hispanics with familial late-onset Alzheimer's diseaseJoseph H Lee, Sandra Barral, Rong Cheng, et al.
Neurogenetics|November 10, 2007
Refinement of the 2p11.1-q12.2 locus responsible for cortical tremor associated with epilepsy and exclusion of candidate genesCécile Saint-Martin, Delphine Bouteiller, Giovanni Stevanin, et al.
Neurogenetics|August 9, 2008
A novel locus for autosomal recessive primary torsion dystonia (DYT17) maps to 20p11.22-q13.12E Chouery, J Kfoury, V Delague, et al.
Neurogenetics|October 14, 2008
A novel mutation in the MFSD8 gene in late infantile neuronal ceroid lipofuscinosisE Stogmann, S El Tawil, J Wagenstaller, et al.
Neurogenetics|July 30, 2008
Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2)Larissa Arning, Ludger Schöls, Huriye Cin, et al.
Neurogenetics|June 20, 2008
Heterogeneous dysregulation of microRNAs across the autism spectrumKawther Abu-Elneel, Tsunglin Liu, Francesca S Gazzaniga, et al.
Pageof 108