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Oxford University Hospitals NHS Foundation Trust

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Molecular Haematology Services

  • Inherited Coagulation Bleeding Disorders (including common FVL/PT genotyping, Haemophilia A, Haemophilia B, VWD, rare bleeding disorders and 40 gene NGS panel)
  • Inherited Platelet Disorders (including Bernard Soulier syndrome, Glanzmann Thrombasthenia, MYH9-related disorders and 57 gene NGS panel)
  • Disorders of Iron Regulation (including common HFE genotyping and 16 gene NGS panel)

Other molecular haematology services in Oxford (including rare anaemias and haemoglobinopathies) are provided by the Oxford Molecular Diagnostics Centre:

Last updated: 26-Feb-2018 by Claire Scott