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American Journal of Mental Retardation : AJMR|June 2, 1998
Phenotypic involvement in females with the FMR1 gene mutationJ E Riddle, A Cheema, W E Sobesky, et al.
Scientific Studies of Reading : the Official Journal of the Society for the Scientific Study of Reading|October 15, 2021
In Search of Cognitive Promotive and Protective Factors for Word ReadingRebecca F Slomowitz, Angela J Narayan, Bruce F Pennington, et al.
Behavior Genetics|January 6, 2011
A family based association study of DRD4, DAT1, and 5HTT and continuous traits of attention-deficit hyperactivity disorderL Cinnamon Bidwell, Erik G Willcutt, Matthew B McQueen, et al.
Human Genetics|May 13, 2004
Refinement of the 6p21.3 quantitative trait locus influencing dyslexia: linkage and association analysesKaren E Deffenbacher, Judith B Kenyon, Denise M Hoover, et al.
Child Development|August 1, 1986
Spelling errors in adults with a form of familial dyslexiaB F Pennington, L L McCabe, S D Smith, et al.
Journal of Exposure Science & Environmental Epidemiology|March 6, 2023
Large-scale agricultural burning and cardiorespiratory emergency department visits in the U.S. state of KansasAudrey F Pennington, Ambarish Vaidyanathan, Farah S Ahmed, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|September 11, 2010
Etiology and neuropsychology of comorbidity between RD and ADHD: the case for multiple-deficit modelsErik G Willcutt, Rebecca S Betjemann, Lauren M McGrath, et al.
New Directions for Child and Adolescent Development|May 10, 2019
Understanding Comorbidity Between Specific Learning DisabilitiesErik G Willcutt, Lauren M McGrath, Bruce F Pennington, et al.
Infection and Immunity|September 20, 2017
H-IPSE Is a Pathogen-Secreted Host Nucleus-Infiltrating Protein (Infiltrin) Expressed Exclusively by the Schistosoma haematobium Egg StageLuke F Pennington, Abdulaziz Alouffi, Evaristus C Mbanefo, et al.
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