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3.4.1 Linkage studies (16)

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14019 Optineurin gene is not involved in the common high-tension form of primary open-angle glaucoma
Ariani F; Longo I; Frezzotti P; Pescucci C; Mari F; Caporossi A; Frezzotti R; Renieri A
Graefe's Archive for Clinical and Experimental Ophthalmology 2006; 244: 1077-1082
14285 Primary congenital glaucoma and Rieger's anomaly: Extended haplotypes reveal founder effects for eight distinct CYP1B1 mutations
Chavarria Soley G; Michels Rautenstrauss K; Pasutto F; Flikier D; Flikier P; Cirak S; Bejjani B; Winters DL; Lewis RA; Mardin C
Molecular Vision 2006; 12: 523-531
14231 Molecular analysis of a human PAX6 homeobox mutant
D'Elia AV; Puppin C; Pellizzari L; Pianta A; Bregant E; Lonigro R; Tell G; Fogolari F; van Heyningen V; Damante-G
European Journal of Human Genetics 2006; 14: 744-751
14160 Lack of association of p53 polymorphisms and haplotypes in high and normal tension open angle glaucoma
Dimasi DP; Hewitt AW; Green CM; Mackey DA; Craig JE
Journal of Medical Genetics 2005; 42: e55
13998 Complex genetics of complex traits: the case of primary open-angle glaucoma
Hewitt AW; Craig JE; Mackey DA
Clinical and Experimental Ophthalmology 2006; 34: 472-484
13965 A glaucoma case-control study of the WDR36 Gene D658G sequence variant
Hewitt AW; Dimasi DP; Mackey DA; Craig JE
American Journal of Ophthalmology 2006; 142: 324-325
14021 Paraoxonase 1 gene polymorphisms influence clinical features of open-angle glaucoma
Inagaki Y; Mashima Y; Funayama T; Ohtake Y; Fuse N; Yasuda N; Fukuchi T; Murakami A; Hotta Y
Graefe's Archive for Clinical and Experimental Ophthalmology 2006; 244: 984-990
13975 The role of the WDR36 gene on chromosome 5q22.1 in a large family with primary open-angle glaucoma mapped to this region
Kramer PL; Samples JR; Monemi S; Sykes R; Sarfarazi M; Wirtz MK
Archives of Ophthalmology 2006; 124: 1328-1331
14156 Heterozygous CYP1B1 gene mutations in Spanish patients with primary open-angle glaucoma
Lopez-Garrido MP; Sanchez-Sanchez F; Lopez-Martinez F; Aroca-Aguilar JD; Blanco-Marchite C; Coca-Prados M; Escribano J
Molecular Vision 2006; 12: 748-755
14163 Methylenetetrahydrofolate reductase gene polymorphisms c.677C/T and c.1298A/C are not associated with open angle glaucoma
Mabuchi F; Tang S; Kashiwagi K; Yamagata Z; Iijima H; Tsukahara S
Molecular Vision 2006; 12: 735-739
14226 A highly complex rea (2;3;11) and aniridia by position effect
Rivera H; Ayala Madrigal ML; Barros Nunez JP; Arnaud Lopez L; Maloney V; Crolla JA
Cytogenetic and Genome Research 2006; 114: 83-88
14055 Genomewide scan and fine mapping of quantitative trait loci for intraocular pressure on 5q and 14q in West Africans
Rotimi CN; Chen G; Adeyemo AA; Jones LS; Agyenim-Boateng K; Eghan BA Jr; Zhou J; Doumatey A; Lashley K; Huang H
Investigative Ophthalmology and Visual Science 2006; 47: 3262-3267
14286 Further support of the role of CYP1B1 in patients with Peters anomaly
Vincent A; Billingsley G; Priston M; Glaser T; Oliver E; Walter M; Ritch R; Levin A; Heon E
Molecular Vision 2006; 12: 506-510
14283 Novel mutations of the PAX6 gene identified in Chinese patients with aniridia
Wang P; Guo X; Jia X; Li S; Xiao X; Zhang Q
Molecular Vision 2006; 12: 644-648
14044 Novel mutations of FOXC1 and PITX2 in patients with Axenfeld-Rieger malformations
Weisschuh N; Dressler P; Schuettauf F; Wolf C; Wissinger B; Gramer E
Investigative Ophthalmology and Visual Science 2006; 47: 3846-3852
14150 Evaluation of the association between OPA1 polymorphisms and primary open-angle glaucoma in Barbados families
Yao W; Jiao X; Hejtmancik JF; Leske MC; Hennis A; Nemesure B; The Barbados Family Study Group
Molecular Vision 2006; 12: 649-654

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