MOLECULAR GENETICS SECTION

The Molecular Genetics Section was established in 1987 and processed around 25,000 samples in 2008. The laboratory is staffed by registered Clinical Scientists, trainee Clinical Scientists, Genetic Technologists and Healthcare Support Workers, under the overall direction of a Consultant Molecular Geneticist.

We employ many different techniques to identify genetic variations at the molecular level. Testing is offered for diseases as diverse as cystic fibrosis (an autosomal recessive single-gene disorder), familial colon cancer (an inherited cancer predisposition syndrome) and chronic myeloid leukaemia (an acquired malignancy of bone marrow & blood cells).

ALL REQUESTS FOR PREDICTIVE / PRE-SYMPTOMATIC ANALYSIS MUST BE MADE VIA CLINICAL GENETICS

Please click here for more information about the genetic tests available for familial cancers or inherited non-cancer disorders.

The molecular genetics section works alongside the oncology cytogenetics section to provide a comprehensive range of tests for acquired malignancies. Please click here for molecular oncology tests.

We also offer a sample export service for tests not available at WMRGL. Samples will be sent to an accredited laboratory whenever possible, but some rare tests may only be available in non-accredited / research laboratories. Onward referral centres can be found through the following portals: www.ukgtn.nhs.uk, www.orpha.net and www.genetests.org

More information about sending samples to the laboratory including opening times can be found here services

Download Molecular Genetics Referral Form

Author: Joanne Mason Authorised by: Fiona Macdonald Version 1.0.7.7
Authorised on 06/01/2010 Next review date 06/01/2011
ONLY VALID ON DAY OF PRINTING