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Clinic at the Royal Children's Hospital

We are specialists in the diagnosis and management of genetic conditions in children and adults. We welcome referrals from GPs and specialists for the assessment, diagnosis and/or management of possible and confirmed genetic conditions in children and adults.

Dr Chloe Cunningham (previously Stutterd), is a Consultant Clinical Geneticist at the Victorian Clinical Genetics Service (VCGS), Principal Investigator in the Molecular Therapies group at the Murdoch Children's Research Institute (MRCI) and Senior Lecturer at the University of Melbourne.

Chloe trained in Paediatrics at the Royal Children's Hospital (RCH) and Clinical Genetics at the VCGS. After specialty training, Chloe completed a three-year Neurogenetics Fellowship with the RCH Department of Neurology and MCRI, and a PhD with the University of Melbourne.

Natasha is a Consultant Clinical Geneticist who completed her training in Paediatrics and Clinical Genetics at the Royal Children’s Hospital and the Victorian Clinical Genetics Services (VCGS).  She completed her PhD through the University of Melbourne in 2015.  Natasha has previously worked as a Consultant Clinical Geneticist in paediatric, adult and prenatal genetics services through Austin Health, the Mercy Hospital for Women and Northern Health.  In 2017, Natasha returned to Parkville when she was appointed as a Consultant Clinical Geneticist at the VCGS and an honorary Clinical Genetic

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