Information brochures

Patient brochures

• Information for patients - English
• Information for patients - Arabic
• Information for patients - Chinese 
• Information for patients - Korean
• Information for patients - Vietnamese

22q11.2 microdeletion news

From December 2021, Sonic Genetics will no longer offer a screen for the 22q11.2 microdeletion as an option with NIPT. 

We are in the process of updating our website and literature. During this process some may still reference the availability of this option. For further information, please contact us.

Information about the specific chromosome conditions

• Trisomy 21 / Downs syndrome 
• Trisomy 18 / Edwards syndrome
• Trisomy 13 / Patau syndrome
• Monosomy X / Turner syndrome
• XXY / Klinefelter syndrome
• Triple X syndrome
• XYY / Jacobs syndrome
• XXYY syndrome

Useful links for patients

• Down Syndrome Australia
• Trisomy Support Group
• What are the types of genetic tests?
• NIPT fact sheet
• Find a Genetic Counsellor

The information on this website is provided for your general information and is not a substitute for the specific advice of your treating doctor.