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Neurogenetics

Showing results (321-330 of 1,080) with videos related to

Pageof 108
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Neurogenetics|April 8, 2022
Identification of a 5 bp duplicate in the AP1S2 gene of an individual with X-linked intellectual disabilityDengna Zhu, Mingmei Wang, Yiran Xu, et al.
Neurogenetics|July 26, 2018
Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelinationTamar Harel, Debra Q Y Quek, Bernice H Wong, et al.
Neurogenetics|December 14, 1999
Genetics of neuroinflammation in Alzheimer diseaseM B Graeber
Neurogenetics|December 14, 1999
Recent developments in the genetics of schizophreniaB S Shastry
Neurogenetics|December 14, 1999
PGL3, a third, not maternally imprinted locus in autosomal dominant paragangliomaS Niemann, D Steinberger, U Müller
Neurogenetics|December 14, 1999
To the readership of neurogenetics
Neurogenetics|February 21, 2006
Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegiaMarcia A Blair, Shaochun Ma, Peter Hedera
Neurogenetics|January 21, 2006
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardationMarco Venturin, Silvia Moncini, Valentina Villa, et al.
Neurogenetics|April 29, 2010
Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, JapanHaruya Sakai, Kunihiro Yoshida, Yusaku Shimizu, et al.
Neurogenetics|September 18, 2009
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosisJanine Kirby, Emily F Goodall, William Smith, et al.
Pageof 108

Showing results (321-330 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|April 8, 2022
Identification of a 5 bp duplicate in the AP1S2 gene of an individual with X-linked intellectual disabilityDengna Zhu, Mingmei Wang, Yiran Xu, et al.
Neurogenetics|July 26, 2018
Homozygous mutation in MFSD2A, encoding a lysolipid transporter for docosahexanoic acid, is associated with microcephaly and hypomyelinationTamar Harel, Debra Q Y Quek, Bernice H Wong, et al.
Neurogenetics|December 14, 1999
Genetics of neuroinflammation in Alzheimer diseaseM B Graeber
Neurogenetics|December 14, 1999
Recent developments in the genetics of schizophreniaB S Shastry
Neurogenetics|December 14, 1999
PGL3, a third, not maternally imprinted locus in autosomal dominant paragangliomaS Niemann, D Steinberger, U Müller
Neurogenetics|December 14, 1999
To the readership of neurogenetics
Neurogenetics|February 21, 2006
Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegiaMarcia A Blair, Shaochun Ma, Peter Hedera
Neurogenetics|January 21, 2006
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardationMarco Venturin, Silvia Moncini, Valentina Villa, et al.
Neurogenetics|April 29, 2010
Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, JapanHaruya Sakai, Kunihiro Yoshida, Yusaku Shimizu, et al.
Neurogenetics|September 18, 2009
Broad clinical phenotypes associated with TAR-DNA binding protein (TARDBP) mutations in amyotrophic lateral sclerosisJanine Kirby, Emily F Goodall, William Smith, et al.
Pageof 108