Neuroscience

Promise seen in possible treatment for autism spectrum disorder

Human chromosome 16p11.2 deletion syndrome is caused by the absence of about 27 genes on chromosome 16. This deletion is characterized by intellectual disability; impaired language, communication, and socialization skills; ...

Genetics

Scientists use advanced imaging to map uncharted area of genome

Using advanced imaging techniques, researchers at the University of Colorado Anschutz Medical Campus have mapped a previously uncharted region of the human genome that gives rise to a variety of disease, setting the stage ...

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