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).
Services provided
VCGS offers a comprehensive range of reproductive screening and diagnostic testing options with expert laboratory and clinical support.
Tests include:
- non -invasive prenatal
- genetic carrier screening
- maternal serum screening
- diagnostic testing to identify chromosomal changes
- newborn screening
- metabolic disorders
- neurogenetic disorders
- cardiac
To see the full range of testing please visit the VCGS .
Eligibility
Contact the VCGS service or discuss with your GP (doctor).