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	Title	Author(s)	Issue Date
	Cerebellar and posterior fossa malformations in patients with autism-associated chromosome 22q13 terminal deletion Journal:American Journal of Medical Genetics, Part A	Aldinger, KA Kogan, J Kimonis, V Fernandez, B Horn, D Klopocki, E Chung, B Toutain, A Weksberg, R Millen, KJ Barkovich, AJ Dobyns, WB	2013
	Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development Journal:Neuron	Lennox, AL Hoye, ML Jiang, R Johnson-Kerner, BL Suit, LA Venkataramanan, S Sheehan, CJ Alsina, FC Fregeau, B Aldinger, KA Moey, C Lobach, I Afenjar, A Babovic-Vuksanovic, D Bezieau, S Blackburn, PR Bunt, J Burglen, L Campeau, PM Charles, P Chung, BHY Cogne, B Curry, C D'Agostino, MD Di Donato, N Faivre, L Heron, D Innes, AM Isidor, B Keren, B Kimball, A Klee, EW Kuentz, P Kury, S Martin-Coignard, D Mirzaa, G Mignot, C Myake, N Matsumoto, N Fujita, A Nava, C Nizon, M Rodriguez, D Blok, LS Thauvin-Robinet, C Thevenon, J Vincent, M Ziegler, A Dobyns, W Richards, LJ Barkovich, AJ Floor, SN Silver, DL Sherr, EH	2020
	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