ey0019.1-9 | Genetics | ESPEYB19
TS Woodring
, MH Mirza
, V Benavides
, KA Ellsworth
, MS Wright
, MJ Javed
, S. Ramiro
Pediatrics. 2021 Jul;148(1):e2020019000. doi: 10.1542/peds.2020-019000.Brief Summary: This case report of an infant with dysgenesis of the corpus callosum, whose whole genome sequencing (WGS) revealed variants of unknown significance (VUS) in ROBO1, demonstrates the potential of VUS in guiding clinical decisions.Next-generation sequencing (NGS) is increasingly...