Victorian Clinical Genetics Services (VCGS) is a specialist prenatal, childhood and adult genetics service. Located on site at The Royal Children’s Hospital (RCH) Melbourne, services include integrated genetic consultations, counselling, testing and diagnostic services for children, adults, families, and prospective parents.
The service is an Australian not-for-profit subsidiary of Murdoch Children’s Research Institute and is located at The Royal Children's Hospital (RCH).
VCGS offers a comprehensive range of reproductive screening and diagnostic testing options with expert laboratory and clinical support.
- non -invasive prenatal
- genetic carrier screening
- maternal serum screening
- diagnostic testing to identify chromosomal changes
- newborn screening
- metabolic disorders
- neurogenetic disorders
To see the full range of testing please visit the VCGS website.
Contact the VCGS service or discuss with your GP (doctor).
How to access
Discuss with your GP or contact 1300 118 247
or call +(03) 8341 6212
or email: firstname.lastname@example.org
Please discuss with your GP or the service staff.