This department provides a diagnostic service for a number of inherited diseases to clinicians in Nottinghamshire, Lincolnshire, Leicestershire, and Southern Derbyshire. In addition, it provides carrier and pre-symptomatic testing, as well as prenatal diagnosis for the Clinical Genetics Service at Nottingham City Hospital and Leicester Royal Infirmary. Individuals interested in carrier or predictive testing are usually first referred to Clinical Genetics for counselling (except for haemochromatosis).
The department can also advise on the appropriateness and availability of tests not provided locally, which may be provided at other centres. DNA can then be extracted from samples and sent on to the appropriate centre.
DNA can also be extracted and stored for future possible testing, if requested.
The department is accredited by UKAS (United Kingdom Accreditation Service) to ISO15189:2012. Further details of accredited services can also be found on the UKAS website (www.ukas.com). The department is also an accredited part of the UK Genetic Testing Network and provides rare disease testing for that network as well as for centres worldwide.
For further information, please contact the department for advice on the appropriateness and availability of tests, clinical indications, and relevant sample requirements. The laboratory can also be contacted for advice on the results and interpretation of individual cases, as well as test limitations and acceptance criteria.
- Sample requirements
- List of Molecular Genetics services and tests available
- Common referral types for the Regional Cytogenetics and Molecular Genetics laboratories
- Contact the laboratory
Click here for a printable user information leaflet (only valid on day of printing): User guide v16.pdf
This department is committed to protecting personal information in accordance with the Nottingham University Hospitals NHS Trust information governance policy.