Auditory evoked M100 response latency is delayed in children with 16p11.2 deletion but not 16p11.2 duplication.
Research Articles
Deletion and duplication of 16p11.2 are associated with opposing effects on visual evoked potential amplitude.
Emergence of a Homo sapiens-specific gene family and chromosome 16p11.2 CNV susceptibility.
16p11.2 deletion and duplication: Characterizing neurologic phenotypes in a large clinically ascertained cohort.
Reductions in synaptic proteins and selective alteration of prepulse inhibition in male C57BL/6 mice after postnatal administration of a VIP receptor (VIPR2) agonist.
Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction.
An AKT3-FOXG1-reelin network underlies defective migration in human focal malformations of cortical development.
Testing sensory and multisensory function in children with autism spectrum disorder.
Atypical processing of voice sounds in infants at risk for autism spectrum disorder.
Dissociation of locomotor and cerebellar deficits in a murine Angelman syndrome model.
- Previous Page
- Viewing
- Next Page