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Reproductive Genetic Testing

percept™ NIPT
prepair™ carrier screening test
Maternal Serum Screening
Prenatal Diagnosis and Pregnancy Loss

Biochemical Genetics

Newborn Bloodspot Screening
Metabolic

Genetics and Genomics

Clinical Exomes
Disorders of Sex Development (DSD)
Neurogenetic Diagnostics
Cardiac Gene Panels
Paediatric Microarray
Single Gene Diagnostics
Cystic Fibrosis Carrier Screening & Diagnostic
Carrier Screening for Spinal Muscular Atrophy (SMA)
Mitochondrial Genetics
Oncology and Chimerism

Newborn Screening

Newborn Screening

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Victorian Clinical Genetics Services

Murdoch Children's Research Institute
Royal Children's Hospital
Flemington Road, Parkville
Victoria 3052 Australia

+61 1300 11 8247
+61 3 8341 6366
[email protected]
ABN: 51 007 032 760

Reproductive Genetic Testing
Biochemical Genetics
- Newborn Bloodspot Screening
- Metabolic

Genetics and Genomics

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Our tests
Our clinics
Core services
About
News
Contact
Collection sites
Order & pay

percept™ non-invasive prenatal test (NIPT)
prepair™ genetic carrier screening test
maternal serum screening and all other VCGS tests