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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.Neurogenetics|May 9, 2003
Apolipoproteins E and C1 and brain morphology in memory impaired eldersJ M Serra-Grabulosa, P Salgado-Pineda, C Junqué, et al.Neurogenetics|May 9, 2003
Significant association of the arylalkylamine N-acetyltransferase ( AA-NAT) gene with delayed sleep phase syndromeHirohiko Hohjoh, Miwa Takasu, Kaori Shishikura, et al.Neurogenetics|March 13, 2008
Differential expression of alpha-synuclein, parkin, and synphilin-1 isoforms in Lewy body diseaseKatrin Beyer, Montserrat Domingo-Sàbat, Jordi Humbert, et al.Pageof 96