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Annals of Neurology|January 1, 1986
Thrombotic cerebral vasculopathy associated with herpes zosterD Eidelberg, A Sotrel, D S Horoupian, et al.Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie|December 22, 1999
A novel PAX6 frameshift mutation in a kindred from Atlantic Canada with familial aniridiaS K Gupta, A Orr, D Bulman, et al.Behavior Genetics|May 1, 1997
Mapping quantitative trait loci for open-field behavior in miceH K Gershenfeld, P E Neumann, C Mathis, et al.Nature Genetics|April 1, 1994
Multifactorial inheritance of neural tube defects: localization of the major gene and recognition of modifiers in ct mutant miceP E Neumann, W N Frankel, V A Letts, et al.Nature Neuroscience|February 27, 2001
PLC-beta1, activated via mGluRs, mediates activity-dependent differentiation in cerebral cortexA J Hannan, C Blakemore, A Katsnelson, et al.Proceedings of the National Academy of Sciences of the United States of America|January 15, 1992
Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophyA H Beggs, P E Neumann, K Arahata, et al.Developmental Biology|February 1, 1990
Analysis of the hotfoot (ho) locus by creation of an insertional mutation in a transgenic mouseJ W Gordon, J Uehlinger, N Dayani, et al.American Journal of Human Genetics|October 16, 1999
Mutations in NPC1 highlight a conserved NPC1-specific cysteine-rich domainW L Greer, M J Dobson, G S Girouard, et al.Genome|September 8, 1998
FISH mapping and inter-Alu fingerprinting define the YAC contig map around the centromeric region of human chromosome 18W L Greer, M J Dobson, P E Neumann, et al.Leukemia|May 23, 2008
Familial essential thrombocythemia with spontaneous megakaryocyte colony formation and acquired JAK2 mutationsJ R Higgs, I Sadek, P E Neumann, et al.Pageof 7