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Edwin J Young

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Journal of Neurodevelopmental Disorders|June 30, 2010
Enhanced prefrontal serotonin 5-HT(1A) currents in a mouse model of Williams-Beuren syndrome with low innate anxietyEliane Proulx, Edwin J Young, Lucy R Osborne, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptomsElaine Tam, Edwin J Young, Colleen A Morris, et al.
Human Mutation|January 15, 2004
Loss of function of the cytoplasmic isoform of the protein laforin (EPM2A) causes Lafora progressive myoclonus epilepsyLeonarda Ianzano, Edwin J Young, Xiao C Zhao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorderKate Tsiplova, Richard M Zur, Christian R Marshall, et al.
American Journal of Human Genetics|May 15, 2012
Duplication of GTF2I results in separation anxiety in mice and humansCarolyn B Mervis, Joana Dida, Emily Lam, et al.
Genome Biology|September 2, 2016
Topoisomerase II beta interacts with cohesin and CTCF at topological domain bordersLiis Uusküla-Reimand, Huayun Hou, Payman Samavarchi-Tehrani, et al.
The New England Journal of Medicine|October 21, 2005
Severe expressive-language delay related to duplication of the Williams-Beuren locusMartin J Somerville, Carolyn B Mervis, Edwin J Young, et al.
The Journal of Clinical Endocrinology and Metabolism|June 14, 2021
Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic FindingsNina Lenherr-Taube, Edwin J Young, Michelle Furman, et al.
Nucleic Acids Research|September 25, 2014
MACE: model based analysis of ChIP-exoLiguo Wang, Junsheng Chen, Chen Wang, et al.
Nature Genetics|September 6, 2003
Mutations in NHLRC1 cause progressive myoclonus epilepsyElayne M Chan, Edwin J Young, Leonarda Ianzano, et al.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
Journal of Neurodevelopmental Disorders|June 30, 2010
Enhanced prefrontal serotonin 5-HT(1A) currents in a mouse model of Williams-Beuren syndrome with low innate anxietyEliane Proulx, Edwin J Young, Lucy R Osborne, et al.
American Journal of Medical Genetics. Part A|June 17, 2008
The common inversion of the Williams-Beuren syndrome region at 7q11.23 does not cause clinical symptomsElaine Tam, Edwin J Young, Colleen A Morris, et al.
Human Mutation|January 15, 2004
Loss of function of the cytoplasmic isoform of the protein laforin (EPM2A) causes Lafora progressive myoclonus epilepsyLeonarda Ianzano, Edwin J Young, Xiao C Zhao, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 5, 2017
A microcosting and cost-consequence analysis of clinical genomic testing strategies in autism spectrum disorderKate Tsiplova, Richard M Zur, Christian R Marshall, et al.
American Journal of Human Genetics|May 15, 2012
Duplication of GTF2I results in separation anxiety in mice and humansCarolyn B Mervis, Joana Dida, Emily Lam, et al.
Genome Biology|September 2, 2016
Topoisomerase II beta interacts with cohesin and CTCF at topological domain bordersLiis Uusküla-Reimand, Huayun Hou, Payman Samavarchi-Tehrani, et al.
The New England Journal of Medicine|October 21, 2005
Severe expressive-language delay related to duplication of the Williams-Beuren locusMartin J Somerville, Carolyn B Mervis, Edwin J Young, et al.
The Journal of Clinical Endocrinology and Metabolism|June 14, 2021
Mild Idiopathic Infantile Hypercalcemia-Part 1: Biochemical and Genetic FindingsNina Lenherr-Taube, Edwin J Young, Michelle Furman, et al.
Nucleic Acids Research|September 25, 2014
MACE: model based analysis of ChIP-exoLiguo Wang, Junsheng Chen, Chen Wang, et al.
Nature Genetics|September 6, 2003
Mutations in NHLRC1 cause progressive myoclonus epilepsyElayne M Chan, Edwin J Young, Leonarda Ianzano, et al.
Pageof 2