Showing results (51-60 of 119) with videos related to
Sort By:
Pageof 12
Eye (London, England)|July 12, 2008
A novel mutation in CRYBB2 responsible for inherited coronary cataractD Lou, J-P Tong, L-Y Zhang, et al.Movement Disorders : Official Journal of the Movement Disorder Society|June 5, 1998
Rarity of debrisoquine hydroxylase gene polymorphism in Chinese patients with Parkinson's diseaseC P Pang, J Zhang, J Woo, et al.The Biochemical Journal|September 15, 1984
Stereochemistry of the incorporation of valine methyl groups into methylene groups in cephalosporin CC P Pang, R L White, E P Abraham, et al.Investigative Ophthalmology & Visual Science|May 8, 2000
Truncations in the TIGR gene in individuals with and without primary open-angle glaucomaD S Lam, Y F Leung, J K Chua, et al.The British Journal of Ophthalmology|August 25, 2001
Rhodopsin mutations in Chinese patients with retinitis pigmentosaW M Chan, K Y Yeung, C P Pang, et al.Eye (London, England)|March 15, 2006
An in vitro study on the compatibility and concentrations of combinations of vancomycin, amikacin, and dexamethasone in human vitreousM Hui, A K H Kwok, C P Pang, et al.Archives of Neurology|April 18, 2000
The alpha-synuclein gene and Parkinson disease in a Chinese populationD K Chan, G Mellick, H Cai, et al.Ophthalmologica. Journal International D'Ophtalmologie. International Journal of Ophthalmology. Zeitschrift Fur Augenheilkunde|December 13, 2001
Congenital hypertrophy of the retinal pigment epithelium and APC mutations in Chinese with familial adenomatous polyposisC P Pang, D S Fan, J W Keung, et al.Biotechniques|March 10, 2001
High-throughput conformation-sensitive gel electrophoresis for discovery of SNPsY F Leung, P O Tam, W C Tong, et al.Pageof 12