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The Diagnostic Genetics department provides a comprehensive genetic service for both inherited and acquired genetic disorders.
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The department uses a wide range of techniques and technologies to identify genetic changes from whole chromosome abnormalities to single nucleotide changes.
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Our portfolio of tests is frequently upgraded to enhance our testing methods to take into account developments in International best practice, technology changes and updated approaches to the interpretation of results.
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Diagnostic Genetics analyses prenatal, post-natal and malignancy samples.
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We perform investigations to provide diagnostic, predictive, prenatal and prognostic information to guide treatment and management of genetic conditions.
Linkages with colleagues in diagnostic and research centres nationally and internationally enable Diagnostic Genetics to be connected to the best technologies and approaches to improve patient care.