RARE-X Introduction
Join Koolen-de Vries Syndrome Foundation and Megan O'Boyle of RARE-X for an introduction to the RARE-X platform. We are very excited about the launch of the KdVS Data Collection Program (DCP). When families contribute data, researchers, doctors and our community can understand more about Koolen-de Vries Syndrome and develop better treatments. This webinar will be […]
