Showing results (791-800 of 1,440) with videos related to
Sort By:
Pageof 144
Molecular Vision|August 4, 2006
A novel mutation in the connexin 46 gene (GJA3) causes autosomal dominant zonular pulverulent cataract in a Hispanic familyP K F Addison, V Berry, K R Holden, et al.BJOG : an International Journal of Obstetrics and Gynaecology|February 21, 2006
Absence of conception after caesarean section: voluntary or involuntary?S Bhattacharya, M Porter, K Harrild, et al.The Journal of Pathology|November 5, 1999
Evolution of genetic abnormalities in hepatocellular carcinomas demonstrated by DNA fingerprintingY Sirivatanauksorn, V Sirivatanauksorn, S Bhattacharya, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|February 7, 2001
Autosomal dominant cone and cone-rod dystrophy with mutations in the guanylate cyclase activator 1A gene-encoding guanylate cyclase activating protein-1S M Downes, G E Holder, F W Fitzke, et al.Transactions of the Ophthalmological Societies of the United Kingdom|January 1, 1983
DNA probes in X-linked retinitis pigmentosaA F Wright, S Bhattacharya, W H Price, et al.BMJ (Clinical Research Ed.)|April 28, 2011
Hysterectomy, endometrial ablation, and levonorgestrel releasing intrauterine system (Mirena) for treatment of heavy menstrual bleeding: cost effectiveness analysisT E Roberts, A Tsourapas, L J Middleton, et al.Cardiovascular Drugs and Therapy|October 1, 1995
Blockade of the human platelet GPIIb/IIIa receptor by a murine monoclonal antibody Fab fragment (7E3): potent dose-dependent inhibition of platelet functionS Bhattacharya, R Jordan, S Machin, et al.Human Molecular Genetics|September 26, 2000
Functional impairment of lens aquaporin in two families with dominantly inherited cataractsP Francis, J J Chung, M Yasui, et al.Gut|October 13, 1999
Genomic heterogeneity in synchronous hepatocellular carcinomasY Sirivatanauksorn, V Sirivatanauksorn, S Bhattacharya, et al.Archives of Ophthalmology (Chicago, Ill. : 1960)|October 26, 1999
Clinical features of codon 172 RDS macular dystrophy: similar phenotype in 12 familiesS M Downes, F W Fitzke, G E Holder, et al.Pageof 144