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Kim Cornish

Showing results (61-70 of 65) with videos related to

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Scientific Reports|June 18, 2024
A digital intervention to support childhood cognition after the COVID-19 pandemic: a pilot trialHannah Kirk, Megan Spencer-Smith, Laura Jobson, et al.
Brain and Cognition|January 16, 2014
Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: through eye movementsAnnie L Shelton, Kim Cornish, Claudine Kraan, et al.
Journal of Autism and Developmental Disorders|November 8, 2013
The interplay between anxiety and social functioning in Williams syndromeDeborah M Riby, Mary Hanley, Hannah Kirk, et al.
Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
Science Translational Medicine|January 7, 2011
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
Pageof 7

Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Scientific Reports|June 18, 2024
A digital intervention to support childhood cognition after the COVID-19 pandemic: a pilot trialHannah Kirk, Megan Spencer-Smith, Laura Jobson, et al.
Brain and Cognition|January 16, 2014
Exploring inhibitory deficits in female premutation carriers of fragile X syndrome: through eye movementsAnnie L Shelton, Kim Cornish, Claudine Kraan, et al.
Journal of Autism and Developmental Disorders|November 8, 2013
The interplay between anxiety and social functioning in Williams syndromeDeborah M Riby, Mary Hanley, Hannah Kirk, et al.
Molecular Autism|May 11, 2019
Incomplete silencing of full mutation alleles in males with fragile X syndrome is associated with autistic featuresEmma K Baker, Marta Arpone, Solange M Aliaga, et al.
Science Translational Medicine|January 7, 2011
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
Pageof 7