Identification of de novo variants in KCTD10 as a proposed cause for multiple congenital anomalies
Titel:
Identification of de novo variants in KCTD10 as a proposed cause for multiple congenital anomalies
Auteur:
Morrow, Michelle M. Torti, Erin McGivern, Bobbi Gates, Ryan Bekheirnia, Mir Reza Bekheirnia, Nasim Folk, Leandra Holtrop, Shannon Palculict, Timothy Blake Redlich, Olivia L. Reich, Adi Guillen Sacoto, Maria J. Shi, Lisong Wentzensen, Ingrid M. McWalter, Kirsty