The number of treatments for rare genetic disorders is expected to increase sharply in the next several years.
Two studies published today in the American Journal of Human Genetics show the potential for genomic screening in newborns to address high rates of infant hospitalization and mortality in the United ...
Expanded carrier screening offers prospective parents the opportunity to assess their risk of passing on genetic disorders by simultaneously testing for a broad array of inherited variants. Initially ...
Florida has launched a newborn genomic screening pilot program designed to test babies for more than 900 genetic conditions, ...
Falling sequencing costs, scalable NGS, robust patient registries and advanced bioinformatics enable higher test volumes, sharper diagnoses and personalized care.Dublin, Sept. (GLOBE NEWSWIRE) -- ...
At Children's Hospital Colorado, Aurora, Colorado, pediatricians will soon have a new ally in diagnosing and identifying complex neurodevelopmental conditions like ...
The Florida Institute for Pediatric Rare Diseases (IPRD) at Florida State University has enrolled its first families in the ...