The Genome Diagnostics Section of the Department of Medical Genetics comprises the Laboratories for DNA diagnostics and Clinical Cytogenetics.

The Genome Diagnostics Section provides both prenatal and postnatal genetic diagnosis using a large variety of state-of-the-art techniques ranging from karyotyping, fluorescent in situ hybridisation, CGH-array to sequencing.

The section combines state-of-the-art genetic testing with comprehensive interpretation of test results by accredited experts to provide accurate, timely molecular and cytogenetic tests for a variety of inherited and congenital disorders.