1. Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes. Issue 1 (22nd October 2022) Authors: Maia, Nuno; Ibarluzea, Nekane; Misra‐Isrie, Mala; Koboldt, Daniel C.; Marques, Isabel; Soares, Gabriela; Santos, Rosário; Marcelis, Carlo L. M.; Keski‐Filppula, Riikka; Guitart, Miriam; Gabau Vila, Elisabeth; Lehman, April; Hickey, Scott; Mori, Mari; Terhal, Paulien; Valenzuela, Irene; Lasa‐Aranz... Journal: American journal of medical genetics Issue: Volume 191:Issue 1(2023) Page Start: 135 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Weak genetic signal for phenotypic integration implicates developmental processes as major regulators of trait covariation. Issue 2 (6th December 2020) Authors: Conith, Andrew J.; Hope, Sylvie A.; Chhouk, Brian H.; Craig Albertson, R. Journal: Molecular ecology Issue: Volume 30:Issue 2(2021) Page Start: 464 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗