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Browsing by Author Curry, CJ

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	Title	Author(s)	Issue Date
	Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: towards recommendation for molecular testing and management Journal:Clinical Genetics	Avila, M Dyment, DA Sagen, JV St-Onge, J Moog, U Chung, BHY Mansour, S Albanese, A Garcia,, S Ortiz Martin, D Lopez, AA Claudi, T König, R White, SM Sawyer, SL Bernstein, JA Slattery, L Jobling, RK Yoon, G Curry, CJ Le Merrer, M Le Luyer, B Héron, D Mathieu-Dramard, M Bitoun, P Odent, S Amiel, J Kuentz, P Thevenon, J Laville, M Reznik, Y Fagour, C Nunes, ML Delesalle, D Manouvrier, S Lascols, O Huet, F Binquet, C Faivre, L Rivière, JB Vigouroux, C Njølstad, PR Innes, AC Thauvin-Robinet, C	2016
	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
	Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations Journal:Journal of Medical Genetics	Aldinger, KA Mendelsohn, NJ Chung, BHY Zhang, W Cohn, DH Fernandez, B Alkuraya, FS Dobyns, WB Curry, CJ	2016

Showing results 1 to 3 of 3