Chromosome 18 Europe
The Chromosome 18 Registry and Research Society (Europe) is a charity set up to bring European families affected by any chromosome 18 abnormalities together to share information and experiences. Our organisation covers all chromosome 18 abnormalities: 18q-, 18p-,Ring 18,Tetrasomy 18p and inversions of chromosome 18.
The charity was founded by an affected woman, her mother and the grandparents of a young boy, all of whom lived near Glasgow. The organisation was registered as a charity in Scotland in 2009 (SC040399). We now have a committee of eight volunteers, all of whom are related to people affected by Chromosome 18 disorders.
About Us
Contact Information
- Phone:
- Email: info@chromosome18eur.org
- Website: http://chromosome18eur.org/
Our Location
Social Media
Display "Featured on PatientGroups.ai" on your site
Help drive awareness to your website
Place this code anywhere on your site, it will link back here: