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Citation: Ma. Pericak-vance et al., A meta-analysis of genomic screens in multiple sclerosis, MULT SCLER, 7(1), 2001, pp. 3-11

Authors: Grimes, DA Bulman, D St George-Hyslop, P Lang, AE

Citation: Da. Grimes et al., Inherited myoclonus-dystonia: Evidence supporting genetic heterogeneity, MOVEMENT D, 16(1), 2001, pp. 106-110

Authors: Damji, KF Sohocki, MM Khan, R Gupta, SK Rahim, M Loyer, M Hussein, N Karim, N Ladak, SS Jamal, A Bulman, D Koenekoop, RK

Citation: Kf. Damji et al., Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p, CAN J OPHTH, 36(5), 2001, pp. 252-259

Authors: Khaliq, Y Gallicano, K Seguin, I Fyke, K Carignan, G Bulman, D Badley, A Cameron, DW

Citation: Y. Khaliq et al., Single and multiple dose pharmacokinetics of nelfinavir and CYP2C19 activity in human immunodeficiency virus-infected patients with chronic liver disease, BR J CL PH, 50(2), 2000, pp. 108-115

Authors: Gupta, SK Orr, A Bulman, D De Becker, L Guernsey, DL Neumann, PE

Citation: Sk. Gupta et al., A novel PAX6 frameshift mutation in a kindred from Atlantic Canada with familial aniridia, CAN J OPHTH, 34(6), 1999, pp. 330-334