1. Expansion and further delineation of the SETD5 phenotype leading to global developmental delay, variable dysmorphic features, and reduced penetrance. Issue 4 (7th January 2018) Authors: Powis, Z.; Farwell Hagman, K.D.; Mroske, C.; McWalter, K.; Cohen, J.S.; Colombo, R.; Serretti, A.; Fatemi, A.; David, K.L.; Reynolds, J.; Immken, L.; Nagakura, H.; Cunniff, C.M.; Payne, K.; Barbaro‐Dieber, T.; Gripp, K.W.; Baker, L.; Stamper, T.; Aleck, K.A.; Jordan, E.S. Journal: Clinical genetics Issue: Volume 93:Issue 4(2018) Page Start: 752 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable features. Issue 5 (10th October 2016) Authors: Cohen, J.S.; Srivastava, S.; Farwell Hagman, K.D.; Shinde, D.N.; Huether, R.; Darcy, D.; Wallerstein, R.; Houge, G.; Berland, S.; Monaghan, K.G.; Poretti, A.; Wilson, A.L.; Chung, W.K.; Fatemi, A. Journal: Clinical genetics Issue: Volume 91:Issue 5(2017) Page Start: 697 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗