Archive: 17/07/2017
Study identifies tools to identify patients at risk for autism spectrum disorders
A tool intended to detect signs of autism in high-risk infants can be used to help identify and treat patients with tuberous sclerosis complex (TSC), a genetic disorder, who most need early intervention. Moreover, they can ...
Jul 17, 2017
A new era in the interpretation of human genomic variation
In a commentary published today in Genetics in Medicine, Heidi Rehm, PhD, highlights the pressing need for standardized human genomic variant interpretation and calls on more stakeholders to join the data sharing movement.
Jul 17, 2017