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Scientific Reports
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June 18, 2024
A digital intervention to support childhood cognition after the COVID-19 pandemic: a pilot trial
Hannah 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 movements
Annie 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 syndrome
Deborah 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 features
Emma 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 AFQ056
Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
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of 7
Search research articles
Search
Showing results (61-70 of 65) with videos related to
Sort By:
Page
of 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 trial
Hannah 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 movements
Annie 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 syndrome
Deborah 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 features
Emma 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 AFQ056
Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
Page
of 7