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	Title	Author(s)	Issue Date
	Mosaic Activating Mutations in FGFR1 Cause Encephalocraniocutaneous Lipomatosis Journal:American Journal of Human Genetics	Bennett, JT Tan, TY Alcantara, D Tetrault, M Timms, AE Jensen, D Collins, S Nowaczyk, MJM Lindhurst, MJ Christensen, KM Braddock, SR Brandling-Bennett, H Hennekam, RCM Chung, BHY Lehman, A Su, J Ng, SY Amor, DJ Majewski, J Biesecker, LG Boycott, KM Dobyns, WB O'Driscoll, M Moog, U McDonell, LM	2016
	Rare SUZ12 variants commonly cause an overgrowth phenotype Journal:American Journal of Medical Genetics Part C: Seminars in Medical Genetics	Cyrus, SS Cohen, ASA Agbahovbe, R Avela, K Yeung, KS Chung, BHY Luk, HM Tkachenko, N Choufani, S Weksberg, R Lopez-Rangel, E Brown, K Sanenz, MS Svihovec, S McCandless, SE Bird, LM Garcia, AG Cambello, MJ McWalter, K Schnur, RE An, J Jones, SJM Bhalla, SK Pinz, H Braddock, SR Gibson, WT	2019
	Redefining the Etiologic Landscape of Cerebellar Malformations Journal:American Journal of Human Genetics	Aldinger, KA Timms, AE Thomson, Z Mirzaa, GM Bennett, JT Rosenberg, AB Roco, CM Hirano, M Abidi, F Haldipur, P Cheng, CV Collins, S Park, K Zeiger, J Overmann, LM Alkuraya, FS Biesecker, LG Braddock, SR Cathey, S Cho, MT Chung, BHY Everman, DB Zarate, YA Jones, JR Schwartz, CE Goldstein, A Hopkin, RJ Krantz, ID Ladda, RL Leppig, KA McGillivray, BC Sell, S Wusik, K Gleeson, JG Nickerson, DA Bamshad, MJ Gerrelli, D Lisgo, SN Seelig, G Ishak, GE Barkovich, AJ Curry, CJ Glass, IA Millen, KJ Doherty, D Dobyns, WB	2019

Showing results 1 to 3 of 3