by Chris Oliver Jo Moss Jane Petty Kate Arron Jenny Sloneem Scott Hall
on behalf of the Cornelia de Lange Syndrome Foundation, published on 20 cze 2003
All of the information on this WebSite is for education purposes only. The place to get specific medical advice, diagnoses, and treatment is your doctor. Use of this site is strictly at your own risk. If you find something that you think needs correction or clarification, please let us know at:
Send a email: info@cdlsWorld.org
info@cdlsworld.org
