fbpx

22q11 Foundation Australia and New Zealand

Description

The 22q Foundation Australia and New Zealand are here to offer practical information, access to research and connections to other families on a similar journey. Whilst our main focus is on 22q11.2 Deletion Syndrome we do offer basic information on other conditions affected by chromosomal abnormalities on the 22nd chromosome in the "q" region. In particular 22q Duplication.​
Type
Online or Phone Service
Alternative Names:
Formerly Shprintzen Syndrome Support Group, VCFS Foundation of NSW
Areas Served:
National
Last review date:
28/12/22

Upgrade Listing

Upgrading the listing is the best way to manage and protect your business.

Upgrade Listing