In this webinar, Suzanne Drury, PhD, Clinical Genomics and Personalized Medicine Specialist at Congenica, highlights the use of Congenica Prenatal™, demonstrating efficient, evidence-based molecular diagnosis of fetal anomalies and the pre-packaged expertise that this application brings. She shares how refined workflows lead to rapid causal variant identification and streamlined reporting.
Watch the webinar to discover:
The diagnostic challenges clinicians face in prenatal settings
How to rapidly identify de novo variants
Maximizing efficiency and diagnostic yield with expert Curated Variant Lists and literature annotations