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1.2 Population genetics (8)
Showing records 1 to 8
Display all abstracts in classification 1.2 Population genetics
Search within classification 1.2 Population genetics6592 Mutations in genes encoding melanosomal proteins cause pigmentary glaucoma in DBA/2J mice
Anderson MG; Smith RS; Hawes NL; Zabaleta A; Chang B; Wiggs JL; John SWM
Nature Genetics 2002; 30: 81-85
6593 Genetic analysis of PITX2 and FOXC1 in Rieger Syndrome patients from Brazil
Borges AS; Susanna R; Carani JCE; Betinjane AJ; Alward WL; Stone EM; Sheffield VC; Nishimura DY
Journal of Glaucoma 2002; 11: 51-56
6594 Differential occurrence of mutations causative of eye diseases in the Chinese population
Chi PP; Lam DSC
Human Mutation 2002; 19: 189-208
6595 Rapid mutation detection by the transgenomic wave analyser DHPLC identifies MYOC mutations in patients with ocular hypertension and/or open angle glaucoma
Cobb CJ; Scott G; Swingler RJ; Wilson S; Ellis J; MacEwen CJ; McLean WHI
British Journal of Ophthalmology 2002; 86: 191-195
6596 MYOC mutation frequency in primary open-angle glaucoma patients from Western Switzerland
Mataftsi A; Achache F; Heon E; Mermoud A; Cousin P; Metthez G; Schorderet DF; Munier FL
Ophthalmic Genetics 2001; 22: 225-231
6597 Adult-onset primary open-angle glaucoma caused by mutations in optineurin
Rezaie T; Child A; Hitchings R; Brice G; Miller L; Coca Prados M; Heon E; Krupin T; Ritch R; Kreutzer D
Science 2002; 295:1077-1079
6598 Myocilin is associated with mitochondria in human trabecular meshwork cells
Wentz Hunter K; Ueda J; Shimizu N; Yue BYJT
Journal of Cellular Physiology 2002; 190: 46-53
6599 Genetic basis of glaucoma
WuDunn D
Current Opinions in Ophthalmology 2002; 13: 55-60