1. Characterizing the phenotypic effect of Xq28 duplication size in MECP2 duplication syndrome. Issue 5 (15th March 2019) Authors: Peters, Sarika U.; Fu, Cary; Suter, Bernhard; Marsh, Eric; Benke, Timothy A.; Skinner, Steve A.; Lieberman, David N.; Standridge, Shannon; Jones, Mary; Beisang, Arthur; Feyma, Timothy; Heydeman, Peter; Ryther, Robin; Kaufmann, Walter E.; Glaze, Daniel G.; Neul, Jeffrey L.; Percy, Alan K. Journal: Clinical genetics Issue: Volume 95:Issue 5(2019) Page Start: 575 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Importance of genetic testing in global health during the evaluation of familial microcephaly. Issue 10 (26th August 2016) Authors: Molinero, Isaac; Broman‐Fulks, Jordan; Lyons, Michael J.; Matheus, Maria Gisele; Chaubey, Alka; DuPont, Barbara R.; Friez, Michael J.; Skinner, Steve A.; Holden, Kenton R. Journal: Clinical case reports Issue: Volume 4:Issue 10(2016) Page Start: 968 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Phenotypic features in MECP2 duplication syndrome: Effects of age. Issue 2 (10th November 2020) Authors: Peters, Sarika U.; Fu, Cary; Marsh, Eric D.; Benke, Tim A.; Suter, Bernard; Skinner, Steve A.; Lieberman, David N.; Standridge, Shannon; Jones, Mary; Beisang, Arthur; Feyma, Timothy; Heydeman, Peter; Ryther, Robin; Glaze, Daniel G.; Percy, Alan K.; Neul, Jeffrey L. Journal: American journal of medical genetics Issue: Volume 185:Issue 2(2021) Page Start: 362 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗