1. A combined RNA-seq and whole genome sequencing approach for identification of non-coding pathogenic variants in single families. (3rd February 2020) Authors: Bronstein, Revital; Capowski, Elizabeth E; Mehrotra, Sudeep; Jansen, Alex D; Navarro-Gomez, Daniel; Maher, Mathew; Place, Emily; Sangermano, Riccardo; Bujakowska, Kinga M; Gamm, David M; Pierce, Eric A Journal: Human molecular genetics Issue: Volume 29:Number 6(2020) Page Start: 967 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗