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  • Autosomal Dominant Polycystic Kidney Disease PKD1/2
  • Autosomal Dominant Polycystic Kidney Disease PKD1/2
  • Autosomal Dominant Polycystic Kidney Disease PKD1/2
  • Autosomal Dominant Polycystic Kidney Disease PKD1/2
  • Congenital thrombotic thrombocytopenic purpura (TTP) / ADAMTS13 deficiency (Upshaw-Schulman Syndrome)
  • Factor V Deficiency
  • Factor XIII Deficiency
  • Fibrinogen Disorders FGA, FGB & FGG Gene Sequencing
  • Glanzmann thrombasthenia
  • Glycogen Storage Disease Next Generation Sequencing Panel: Liver
  • Haemophilia A & B/Factor IX deficiency
  • Haemophilia A & B/Factor IX deficiency
  • Haemophilia A & B/Factor IX deficiency
  • Haemophilia A & B/Factor IX deficiency
  • Haemophilia A & B/Factor IX deficiency
  • Haemophilia A & B/Factor IX deficiency
  • Haemophilia A/Factor VIII deficiency
  • Haemophilia A/Factor VIII deficiency
  • Haemophilia A/Factor VIII deficiency
  • Haemophilia A/Factor VIII deficiency
  • Haemophilia A/Factor VIII deficiency
  • Haemophilia A/Factor VIII deficiency
  • Haemophilia A/Factor VIII deficiency
  • Hereditary Spastic Paraparesis (HSP)
  • Hereditary Spastic Paraparesis (HSP)
  • Hereditary Spastic Paraparesis (HSP)
  • Hereditary Spastic Paraparesis (HSP)
  • Metabolic Myopathies / Rhabdomyolysis
  • Multiple Endocrine Neoplasia Type 1 MEN1 gene
  • Multiple Endocrine Neoplasia Type 1 MEN1 gene
  • Multiple Endocrine Neoplasia Type 1 MEN1 gene
  • Multiple Endocrine Neoplasia Type 1 MEN1 gene
  • Multiple Endocrine Neoplasia Type 1 MEN1 gene
  • MYH9 Macrothrombocytopenia
  • Osteogenesis Imperfecta, Autosomal Dominant
  • von Willebrand Disease
  • von Willebrand Disease
  • Wilson disease (ATP7B)

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    News

    Transactional website goes live offering specialist genetic testing

     

    First tests to go live are Glycogen Storage Disease Next Generation Sequencing Panels: Liver, Metabolic Myopathies / Rhabdomyolysis & Wilson Disease. 

    Keep a look out for more tests added soon!
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