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K G Wigg

Showing results (11-20 of 17) with videos related to

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American Journal of Medical Genetics|February 25, 2000
Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorderC L Barr, K G Wigg, J Wu, et al.
Genes, Brain, and Behavior|October 3, 2006
Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorderK M Dorval, K G Wigg, J Crosbie, et al.
Genes, Brain, and Behavior|March 12, 2014
Association of the ROBO1 gene with reading disabilities in a family-based analysisC Tran, K G Wigg, K Zhang, et al.
Molecular Psychiatry|February 21, 2007
Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problemsP Luca, N Laurin, V L Misener, et al.
Molecular Psychiatry|July 14, 2004
Support for EKN1 as the susceptibility locus for dyslexia on 15q21K G Wigg, J M Couto, Y Feng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 24, 2013
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1C Tran, F Gagnon, K G Wigg, et al.
Neuropsychobiology|October 4, 2008
Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disordersV L Misener, L Gomez, K G Wigg, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
American Journal of Medical Genetics|February 25, 2000
Linkage study of two polymorphisms at the dopamine D3 receptor gene and attention-deficit hyperactivity disorderC L Barr, K G Wigg, J Wu, et al.
Genes, Brain, and Behavior|October 3, 2006
Association of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorderK M Dorval, K G Wigg, J Crosbie, et al.
Genes, Brain, and Behavior|March 12, 2014
Association of the ROBO1 gene with reading disabilities in a family-based analysisC Tran, K G Wigg, K Zhang, et al.
Molecular Psychiatry|February 21, 2007
Association of the dopamine receptor D1 gene, DRD1, with inattention symptoms in families selected for reading problemsP Luca, N Laurin, V L Misener, et al.
Molecular Psychiatry|July 14, 2004
Support for EKN1 as the susceptibility locus for dyslexia on 15q21K G Wigg, J M Couto, Y Feng, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|January 24, 2013
A family-based association analysis and meta-analysis of the reading disabilities candidate gene DYX1C1C Tran, F Gagnon, K G Wigg, et al.
Neuropsychobiology|October 4, 2008
Cytokine Genes TNF, IL1A, IL1B, IL6, IL1RN and IL10, and childhood-onset mood disordersV L Misener, L Gomez, K G Wigg, et al.
Pageof 2