Rare-X Webinar

Join us to learn more about how you can contribute to the new Pallister-Killian Syndrome data collection program.  It is all online.  This is exciting new as it will help doctors and scientists around the world have access to traits and symptoms of PKS.  Here is the link to the webinar: http://tiny.cc/pkskids

Thank you for joining us for this exciting next step for PKS Kids!