Abnormal auditory and language pathways in children with 16p11.2 deletion.
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Clinical phenotype of the recurrent 1q21.1 copy-number variant.
Genotype-first analysis of the 16p11.2 deletion defines a new type of “autism.”
The cognitive and behavioral phenotype of the 16p11.2 deletion in a clinically ascertained population.
Modulation of mu attenuation to social stimuli in children and adults with 16p11.2 deletions and duplications.
A potential contributory role for ciliary dysfunction in the 16p11.2 600 kb BP4-BP5 pathology.
The role of parental cognitive, behavioral, and motor profiles in clinical variability in individuals with chromosome 16p11.2 deletions.
Maternal modifiers and parent-of-origin bias of the autism-associated 16p11.2 CNV.
A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.
Autism spectrum disorder, developmental and psychiatric features in 16p11.2 duplication.
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