Elevating laboratory workflow: NHS Scotland implemented Devyser FH NGS for improved speed and clinical precision
Meet Silvia Borras, a Development Lead and Clinical Scientist in Genetics and Molecular Pathology...
In this webinar, Prof. Albert Wiegman (MD, PhD), paediatric cardiologist at Amsterdam UMC, talks about how early paediatric screening and genetic testing can guide detection and treatment of familial hypercholesterolemia (FH).
Currently, FH is diagnosed later in life at an median age of 44. In the webinar, Prof. Wiegman details how early cholesterol screening and genetic testing in children can improve patient outcomes and provide a cost-effective treatment strategy.
Meet Silvia Borras, a Development Lead and Clinical Scientist in Genetics and Molecular Pathology...
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As a lab manager, you know the importance of streamlining workflows to maximize productivity and...
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An expert consensus panel has recently promoted genetic testing for Familial Hypercholesterolemia...
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