Info About the TSRR Registry
The Turner Syndrome Research Registry (TSRR) is dedicated to Turner syndrome research. The TSRR is a private and secure way to collect TS related health care information from participants and allows TS researchers to connect with you or information about you. The Registry system built on the PEER (People Engaging Everyone Responsibly) platform created by Genetic Alliance. It only takes the participants 15 minutes to register and complete the initial survey.