Interstitial 20p13 microdeletion including PRNP and adjacent genes in a fetus with congenital abnormalities-First case report.
Pelin OnurMary ShaverMohammed Anwaruddin IqbalPublished in: Clinical case reports (2021)
We present a prenatal case with congenital anomalies that revealed a 759 kb microdeletion at 20p13 possibly implicating PRNP and adjacent genes.