From preconception to parenthood, our advanced genetic testing and expert guidance help build healthier families.
Explore our servicesWhat we do
We offer a wide range of genetic tests and specialist support at every stage — from preconception planning to pregnancy, fetal evaluation and beyond.
Understand genetic risks before pregnancy.
Carrier screening looks at whether you and your partner carry the same inherited condition, such as thalassaemia or spinal muscular atrophy, before a pregnancy begins. Most carriers are healthy with no family history, so the result is often the first sign of a risk, and lets you plan with confidence.
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Early and accurate insights during pregnancy.
From the first trimester, screening estimates the chance of common chromosomal conditions using biochemistry, ultrasound markers and cell-free fetal DNA from a blood draw. Where a result needs confirming, diagnostic testing on a CVS or amniotic fluid sample gives a definitive answer.
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Advanced testing for fetal anomalies and genetic conditions.
When an ultrasound raises a concern, fetal genetic testing helps explain why. Karyotyping looks at the number and structure of the chromosomes, microarray finds small imbalances it can miss, and sequencing reads the genes themselves, interpreted by our teams for informed decisions.
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Our genetic counsellors will walk you and your clinician through the right pathway.
