top of page

The More You Know: Genetic Testing

The Kabuki Syndrome community is invited to join us for a 30 minute Zoom/Webinar reviewing all things related to genetic testing, with a FOCUS on Kabuki Syndrome genetic test reports.


This webinar is pertaining to general information. Patient specific questions cannot be discussed. Have questions but not able to attend? Email questions to kabuki@childrens.harvard.edu in advance and watch the webinar later. The recorded session will be posted on royakabuki.org and allthingskabuki.org.


Shout out to Dr. Olaf Bodamer and his team for making this resource available to our community.



 
 
 

Comments


MAKE A TAX DEDUCTIBLE DONATION TODAY!
EIN #: 47-5441487
  • Twitter - White Circle
  • Facebook - White Circle
  • White Instagram Icon
  • YouTube - White Circle
platinum.jpg
NORD_MembershipLogo_Platinum 2021.png
All Things Kabuki (ATK) is a registered 501(c)3 non-profit corporation based out of Wasilla, Alaska. We are the only U.S. patient advocacy group supporting the Kabuki community globally. Our mission is to raise awareness, incite research, and support individuals and families affected by Kabuki Syndrome.

© 2013-2025 ALL THINGS KABUKI

bottom of page