Use precise geolocation data and actively scan device characteristics for identification. This is done to store and access ...

Scientists have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.

A toddler was successfully treated for a rare genetic disease, spinal muscular atrophy, after world-first in-womb therapy.

Scientists at the Icahn School of Medicine at Mount Sinai and collaborators have identified novel genetic interactions that may contribute to congenital heart disease (CHD), a common birth defect.

Gene therapy represents a paradigm shift in modern medicine, offering unprecedented opportunities to combat diseases at their ...

Four-week-old Tommy Parry is one of only 23 in the world ever to be born with the mitochondrial gene, which impairs his ...

Medical genetics department expands services, designated as Centre of Excellence under National Policy for Rare Diseases.