Register now for “Ask-a-Researcher” with Dr. Rosanna Weksberg

Announcements and updates
Written By Amanda Johnson

Join Dr. Rosanna Weksberg and her research team from the Hospital for Sick Kids and the University of Toronto for a live presentation on Thursday, September 23 at 12pm Eastern about their study of ASXL1 and ASXL3, the genes that cause Bohring-Opitz Syndrome and Bainbridge-Ropers Syndrome. With support of an ARRE Foundation research grant, Dr. Weksberg is studying the patterns of DNA methylation, or signatures, associated with changes in the ASXL genes.

The session is intended for families and all are welcome to join.

Amanda Johnson
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