Artwork
iconShare
 
Manage episode 492479307 series 3253844
Content provided by HudsonAlpha Institute for Biotechnology. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by HudsonAlpha Institute for Biotechnology or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://staging.podcastplayer.com/legal.

When more than 20 children worldwide developed similar neurodevelopmental symptoms, scientists turned to DNA for answers. In this episode, we explore how researchers used innovative genetic tools—and a little matchmaking—to identify variants in the gene ZMYM3 as a potential cause. Go behind the scenes in the lab to see how science is ending diagnostic odysseys for families around the world.

To go behind the scenes and learn more about this episode, visit "DNA Clues: Diagnosing the Undiagnosed."

Thanks for listening! We're now on YouTube- follow us here. To receive episode updates and bonus material, subscribe to our mailing list here.

  continue reading

47 episodes