Pages that link to "Q38246338"
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The following pages link to Autism and fragile X syndrome (Q38246338):
Displaying 14 items.
- Molecular Correlates and Recent Advancements in the Diagnosis and Screening of FMR1-Related Disorders (Q28077980) (← links)
- The fragile X mental retardation 1 gene (FMR1): historical perspective, phenotypes, mechanism, pathology, and epidemiology (Q30249226) (← links)
- Matrix metalloproteinase-9 deletion rescues auditory evoked potential habituation deficit in a mouse model of Fragile X Syndrome (Q30357779) (← links)
- Serum glycopattern and Maackia amurensis lectin-II binding glycoproteins in autism spectrum disorder (Q33651921) (← links)
- Effects of a social stimulus on gene expression in a mouse model of fragile X syndrome (Q33827442) (← links)
- Shared functional defect in IP₃R-mediated calcium signaling in diverse monogenic autism syndromes (Q37347754) (← links)
- The mTOR signalling cascade: paving new roads to cure neurological disease (Q38875632) (← links)
- Autism Symptoms in Fragile X Syndrome. (Q39375314) (← links)
- Treating a novel plasticity defect rescues episodic memory in Fragile X model mice (Q46229249) (← links)
- Autism Spectrum Disorder Symptoms in Infants with Fragile X Syndrome: A Prospective Case Series (Q47960612) (← links)
- Stranger Fear and Early Risk for Social Anxiety in Preschoolers with Fragile X Syndrome Contrasted to Autism Spectrum Disorder (Q47986473) (← links)
- Home-cage hypoactivity in mouse genetic models of autism spectrum disorder (Q91850695) (← links)
- Distance delivery of a parent-implemented language intervention for young boys with fragile X syndrome (Q92992786) (← links)
- Molecular analysis of FMR1 gene in a population in Southern Brazil: Comparison of four methods (Q95278253) (← links)