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Gene-Access is a comprehensive carrier screening service for cystic fibrosis, fragile X syndrome and spinal muscular atrophy.
Click here to view moreOur Cystic Fibrosis Carrier Screening Kit contains everything required to submit a painless cheek swab sample to clarify risk and help couples minimise the chances of passing this condition to their offspring.
Click here to view moreHarmony Prenatal Test is a new type of screening test that analyses this DNA in a sample of your blood to assess the risk of Down syndrome (trisomy 21) and two other genetic conditions, trisomy 18 (Edwards syndrome) and trisomy 13 (Patau syndrome).
Click here to view moreFirst Trimester Screening is used to identify women with an increased risk of having an affected foetus with chromosomal aneuploidy such as Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18) or Patau syndrome (Trisomy 13).
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