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D F Newbury

Showing results (1-10 of 11) with videos related to

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Neuron|October 20, 2010
Genetic advances in the study of speech and language disordersD F Newbury, A P Monaco
Cytogenetic and Genome Research|March 17, 2009
Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assaysL Winchester, D F Newbury, A P Monaco, et al.
Genes, Brain, and Behavior|November 17, 2007
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairmentM Falcaro, A Pickles, D F Newbury, et al.
Molecular Psychiatry|March 15, 2017
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disordersP Devanna, X S Chen, J Ho, et al.
Behavior Genetics|December 18, 2010
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjectsD F Newbury, S Paracchini, T S Scerri, et al.
Genes, Brain, and Behavior|March 30, 2010
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3L Addis, A D Friederici, S A Kotz, et al.
American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Genes, Brain, and Behavior|March 18, 2015
Lack of replication for the myosin-18B association with mathematical ability in independent cohortsK A Pettigrew, S F Fajutrao Valles, K Moll, et al.
Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Neuron|October 20, 2010
Genetic advances in the study of speech and language disordersD F Newbury, A P Monaco
Cytogenetic and Genome Research|March 17, 2009
Detection, breakpoint identification and detailed characterisation of a CNV at the FRA16D site using SNP assaysL Winchester, D F Newbury, A P Monaco, et al.
Genes, Brain, and Behavior|November 17, 2007
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairmentM Falcaro, A Pickles, D F Newbury, et al.
Molecular Psychiatry|March 15, 2017
Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disordersP Devanna, X S Chen, J Ho, et al.
Behavior Genetics|December 18, 2010
Investigation of dyslexia and SLI risk variants in reading- and language-impaired subjectsD F Newbury, S Paracchini, T S Scerri, et al.
Genes, Brain, and Behavior|March 30, 2010
A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3L Addis, A D Friederici, S A Kotz, et al.
American Journal of Human Genetics|March 15, 2002
FOXP2 is not a major susceptibility gene for autism or specific language impairmentD F Newbury, E Bonora, J A Lamb, et al.
Genes, Brain, and Behavior|February 28, 2014
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairmentR Nudel, N H Simpson, G Baird, et al.
Genes, Brain, and Behavior|March 18, 2015
Lack of replication for the myosin-18B association with mathematical ability in independent cohortsK A Pettigrew, S F Fajutrao Valles, K Moll, et al.
Genes, Brain, and Behavior|July 29, 2014
Genome-wide screening for DNA variants associated with reading and language traitsA Gialluisi, D F Newbury, E G Wilcutt, et al.
Pageof 2