Skip to the content

Uniparental disomy in a population of 32,067 clinical exome trios

GeneDx Admin | January 25, 2021

Trio exome sequencing (ES) presents a comprehensive method for detection of UPD alongside sequence and copy-number variant analysis.

Categories:

Post navigation

← Evidence for 28 genetic disorders discovered by combining healthcare and research data
Molecular Diagnostic Yield of Exome Sequencing in Patients With Cerebral Palsy →