De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea.
Research Articles
No increase in autism associated genetic events in children conceived by assisted reproductive technology.
Nonverbal and verbal cognitive discrepancy profiles in autism spectrum disorders: Influence of age and gender.
Expression of the broad autism phenotype in simplex autism families from the Simons Simplex Collection.
De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.
Language impairment and dyslexia genes influence language skills in children with autism spectrum disorders.
CRISPR-CAS9 knockin mice for genome editing and cancer modeling.
Behavioral abnormalities and circuit defects in the basal ganglia of a mouse model of 16p11.2 deletion syndrome.
Intracellular mGluR5 can mediate synaptic plasticity in the hippocampus.
MET receptor tyrosine kinase controls dendritic complexity, spine morphogenesis, and glutamatergic synapse maturation in the hippocampus.
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