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Neuron
|
October 20, 2010
Genetic advances in the study of speech and language disorders
D 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 assays
L 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 impairment
M 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 disorders
P 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 subjects
D 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-q14.3
L 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 impairment
D 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 impairment
R 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 cohorts
K 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 traits
A Gialluisi, D F Newbury, E G Wilcutt, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Neuron
|
October 20, 2010
Genetic advances in the study of speech and language disorders
D 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 assays
L 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 impairment
M 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 disorders
P 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 subjects
D 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-q14.3
L 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 impairment
D 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 impairment
R 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 cohorts
K 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 traits
A Gialluisi, D F Newbury, E G Wilcutt, et al.
Page
of 2