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1.2 Population genetics (14)
Showing records 1 to 14
Display all abstracts in classification 1.2 Population genetics
Search within classification 1.2 Population genetics3363 Investigating the association between OPA1 polymorphisms and glaucoma: comparison between normal tension and high tension primary open angle glaucoma
Aung T; Ocaka L; Ebenezer ND; Morris AG; Brice G; Child AH; Hitchings RA; Lehmann OJ; Bhattacharya SS
Human Genetics 2002; 110: 513-514
3697 A major marker for normal tension glaucoma: association with polymorphisms in the OPA1 gene
Aung T; Ocaka L; Ebenezer ND; Morris AG; Krawczak M; Thiselton; Dawn L; Alexander C; Votruba M; Brice G
Human Genetics 2002; 110: 52-56
3365 Apolipoprotein E-promoter single-nucleotide polymorphisms affect the phenotype of primary open-angle glaucoma and demonstrate interaction with the myocilin gene
Copin B; Brezin AP; Valtot F; Dascotte JC; Bechetoille A; Garchon HJ
American Journal of Human Genetics 2002; 70: 1575-1581
3366 Study on single nucleotide polymorphism of TIGR gene in primary open-angle glaucoma patients
Fan B; Liang X; Peng Z; Dong X; Liu Y; Luan J; Wang N
Zhonghua Yi Xue Za Zhi 2002; 82: 743-747
3367 Anterior segment dysgenesis and the developmental glaucomas are complex traits
Gould DB; John SWM
Human Molecular Genetics 2002; 11: 1185-1193
3368 Myocilin mutations in a population-based sample of cases with open-angle glaucoma: the Rotterdam study
Hulsman CA; De Jong PT; Lettink M; Van Duijn CM; Hofman A; Bergen AA
Graefe's Archive for Clinical and Experimental Ophthalmology 2002; 240: 468-474
3698 Ocular developmental abnormalities and glaucoma associated with interstitial 6p25 duplications and deletions
Lehmann OJ; Ebenezer ND; Ekong R; Ocaka L; Mungall AJ; Fraser S; McGill JI; Hitchings RA; Khaw PT; Sowden JC
Investigative Ophthalmology and Visual Science 2002; 43: 1843-1849
3370 Molecular genetics of Axenfeld-Rieger malformations
Lines MA; Kozlowski K; Walter MA
Human Molecular Genetics 2002; 11: 1177-1184
3371 DNA sequence variants in the tyrosinase-related protein 1 (TYRP1) gene are not associated with human pigmentary glaucoma
Lynch S; Yanagi G; Delbono E; Wiggs JL
Molecular Vision 2002; 8: 127-129
3372 Foxe3 haploinsufficiency in mice: a model for Peters' anomaly
Ormestad M; Blixt Å; Churchill A; Martinsson T; Enerbäck S; Carlsson P
Investigative Ophthalmology and Visual Science 2002; 43: 1350-1357
3373 Identification of novel mutations causing familial primary congenital glaucoma in Indian pedigrees
Panicker SG; Reddy ABM; Mandal AK; Ahmed N; Nagarajaram HA; Hasnain SE; Balasubramanian D
Investigative Ophthalmology and Visual Science 2002; 43: 1358-1366
3374 Molecular genetics of primary congenital glaucoma in Brazil
Stoilov IR; Costa VP; Vasconcellos JPC; Melo MB; Betinjane AJ; Carani JCE; Oltrogge EV; Sarfarazi M
Investigative Ophthalmology and Visual Science 2002; 43: 1820-1827
3375 Two families with primary open-angle glaucoma associated with myocilin gene mutations
Takahashi H; Ohtake Y; Kubota R; Kimura I; Miyata H; Miyata K; Tanino T; Mashima Y
Nippon Ganka Gakkai Zasshi 2002; 106: 201-207
3376 Optimedin: a novel olfactomedin-related protein that interacts with myocilin
Torrado M; Trivedi R; Zinovieva R; Karavanova I; Tomarev SI
Human Molecular Genetics 2002; 11: 1291-1301
