De novo and inherited variants in DDX39B cause a Novel Syndrome Characterized by Neurodevelopmental Delay, Short Stature, and Congenital Hypotonia https://www.medrxiv.org/content/10.1101/2023.07.15.23292630
De novo and inherited variants in DDX39B cause a Novel Syndrome Characterized by Neurodevelopmental Delay, Short Stature, and Congenital Hypotonia https://www.medrxiv.org/content/10.1101/2023.07.15.23292630