This is the first step towards the use of gene editing therapies to treat a wide variety of rare genetic disorders for which ...

In a world first, scientists used CRISPR to fix a baby's unique genetic mutation. The report offers hope for personalized ...

The technique used on a 9½-month-old boy with a rare condition has the potential to help people with thousands of other ...

After Andy Sandness was left with devastating facial injuries, he became the recipient of one of the most complex face ...

While thousands linger on organ waiting lists, the national transplant network is ditching 40-year-old systems and struggling ...