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J R Gruen

Showing results (11-20 of 20) with videos related to

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Genomics|November 15, 2001
Peaks of linkage are localized by a BAC/PAC contig of the 6p reading disability locusJ Ahn, T W Won, A Zia, et al.
Developmental Cognitive Neuroscience|June 13, 2018
Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexiaT M Centanni, D Pantazis, D T Truong, et al.
Genomics|October 1, 1992
Physical and genetic mapping of the telomeric major histocompatibility complex region in man and relevance to the primary hemochromatosis gene (HFE)J R Gruen, V L Goei, K M Summers, et al.
Human Mutation|April 11, 2001
Human GABA(B) receptor 1 gene: eight novel sequence variantsF M Hisama, J R Gruen, J Choi, et al.
American Journal of Human Genetics|June 1, 1997
Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomesR S Ajioka, L B Jorde, J R Gruen, et al.
Genes, Brain, and Behavior|March 18, 2015
The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domainsJ D Eicher, C M Stein, F Deng, et al.
American Journal of Human Genetics|April 16, 2002
Evidence for linkage and association with reading disability on 6p21.3-22D E Kaplan, J Gayán, J Ahn, et al.
Human Genetics|August 19, 2016
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disordersD T Truong, L D Shriberg, S D Smith, et al.
Genomics|August 15, 1996
A transcription map of the major histocompatibility complex (MHC) class I regionJ R Gruen, S R Nalabolu, T W Chu, et al.
Genes, Brain, and Behavior|September 13, 2013
Genome-wide association study of shared components of reading disability and language impairmentJ D Eicher, N R Powers, L L Miller, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Genomics|November 15, 2001
Peaks of linkage are localized by a BAC/PAC contig of the 6p reading disability locusJ Ahn, T W Won, A Zia, et al.
Developmental Cognitive Neuroscience|June 13, 2018
Increased variability of stimulus-driven cortical responses is associated with genetic variability in children with and without dyslexiaT M Centanni, D Pantazis, D T Truong, et al.
Genomics|October 1, 1992
Physical and genetic mapping of the telomeric major histocompatibility complex region in man and relevance to the primary hemochromatosis gene (HFE)J R Gruen, V L Goei, K M Summers, et al.
Human Mutation|April 11, 2001
Human GABA(B) receptor 1 gene: eight novel sequence variantsF M Hisama, J R Gruen, J Choi, et al.
American Journal of Human Genetics|June 1, 1997
Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomesR S Ajioka, L B Jorde, J R Gruen, et al.
Genes, Brain, and Behavior|March 18, 2015
The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domainsJ D Eicher, C M Stein, F Deng, et al.
American Journal of Human Genetics|April 16, 2002
Evidence for linkage and association with reading disability on 6p21.3-22D E Kaplan, J Gayán, J Ahn, et al.
Human Genetics|August 19, 2016
Multipoint genome-wide linkage scan for nonword repetition in a multigenerational family further supports chromosome 13q as a locus for verbal trait disordersD T Truong, L D Shriberg, S D Smith, et al.
Genomics|August 15, 1996
A transcription map of the major histocompatibility complex (MHC) class I regionJ R Gruen, S R Nalabolu, T W Chu, et al.
Genes, Brain, and Behavior|September 13, 2013
Genome-wide association study of shared components of reading disability and language impairmentJ D Eicher, N R Powers, L L Miller, et al.
Pageof 2