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Neurogenetics

Showing results (91-100 of 1,080) with videos related to

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Neurogenetics|March 30, 2019
Pathogenic variants in AIMP1 cause pontocerebellar hypoplasiaAndrea Accogli, Laura Russell, Guillaume Sébire, et al.
Neurogenetics|August 28, 2025
Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 geneRobin A Pilz, Matthias Begemann, Surema Pfister, et al.
Neurogenetics|May 11, 2020
Rare copy number variations of planar cell polarity genes are associated with human neural tube defectsTian Tian, Yunping Lei, Yongyan Chen, et al.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Neurogenetics|July 2, 2003
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locusDésirée von Tell, Carl E G Bruder, Louise V B Anderson, et al.
Neurogenetics|May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonatesA De Luca, M Rizzardi, I Torrente, et al.
Neurogenetics|May 17, 2001
Ataxin-7 expression analysis in controls and spinocerebellar ataxia type 7 patientsD D Einum, J J Townsend, L J Ptácek, et al.
Neurogenetics|May 17, 2001
Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of strokeR P De Lange, K Burr, J S Clark, et al.
Neurogenetics|November 21, 2000
The parental origin of new mutations in neurofibromatosis 2L Kluwe, V Mautner, D M Parry, et al.
Neurogenetics|November 21, 2000
Supporting evidence of a gene for partial epilepsy on 10qV F Mautner, M Lindenau, A Gottesleben, et al.
Pageof 108

Showing results (91-100 of 1,080) with videos related to

Sort By:
Pageof 108
Neurogenetics|March 30, 2019
Pathogenic variants in AIMP1 cause pontocerebellar hypoplasiaAndrea Accogli, Laura Russell, Guillaume Sébire, et al.
Neurogenetics|August 28, 2025
Familial cerebral cavernous malformations caused by a novel germline structural variant in the KRIT1 geneRobin A Pilz, Matthias Begemann, Surema Pfister, et al.
Neurogenetics|May 11, 2020
Rare copy number variations of planar cell polarity genes are associated with human neural tube defectsTian Tian, Yunping Lei, Yongyan Chen, et al.
Neurogenetics|May 29, 2020
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizuresReeval Segel, Adi Aran, Suleyman Gulsuner, et al.
Neurogenetics|July 2, 2003
Refined mapping of the Welander distal myopathy region on chromosome 2p13 positions the new candidate region telomeric of the DYSF locusDésirée von Tell, Carl E G Bruder, Louise V B Anderson, et al.
Neurogenetics|May 17, 2001
Dopamine D4 receptor (DRD4) polymorphism and adaptability trait during infancy: a longitudinal study in 1- to 5-month-old neonatesA De Luca, M Rizzardi, I Torrente, et al.
Neurogenetics|May 17, 2001
Ataxin-7 expression analysis in controls and spinocerebellar ataxia type 7 patientsD D Einum, J J Townsend, L J Ptácek, et al.
Neurogenetics|May 17, 2001
Mapping and sequencing rat dishevelled-1: a candidate gene for cerebral ischaemic insult in a rat model of strokeR P De Lange, K Burr, J S Clark, et al.
Neurogenetics|November 21, 2000
The parental origin of new mutations in neurofibromatosis 2L Kluwe, V Mautner, D M Parry, et al.
Neurogenetics|November 21, 2000
Supporting evidence of a gene for partial epilepsy on 10qV F Mautner, M Lindenau, A Gottesleben, et al.
Pageof 108