This research highlights the scale and clinical impact of GeneDx Infinity™ - the largest and most comprehensive rare disease genomic dataset - and GeneDx's leadership in bringing exome and genome ...
A systematic review of 52 scientific papers submitted to a world-leading clinical genetics journal from multiple scientists ...
BACKGROUND: Sarcomere gene variants are a key cause of hypertrophic cardiomyopathy (HCM), and have been associated with worse prognosis. However, it is unclear how comorbidities influence clinical ...
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