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9.1.1 Congenital glaucoma, Buphthalmos (6)
Showing records 1 to 6
Display all abstracts in classification 9.1.1 Congenital glaucoma, Buphthalmos
Search within classification 9.1.1 Congenital glaucoma, Buphthalmos47948 Compound heterozygous mutations in PYCR1 further expand the phenotypic spectrum of De Barsy syndrome
Lin D-S; Chang J-H; Liu H-L; Wei C-H; Yeung C-Y; Ho C-S; Shu C-H; Chiang M-F; Chuang C-K; Huang Y-W
American Journal of Medical Genetics, Part A 2011; 155: 3095-3099
47827 Mutation spectrum of CYP1B1 and MYOC genes in Korean patients with primary congenital glaucoma
Kim H-J; Suh W; Park SC; Kim CY; Park KH; Kook MS; Kim YY; Kim C-s; Park CK; Ki C-S
Molecular Vision 2011; 17: 2093-2101
47627 CYP1B1-related anterior segment developmental anomalies: Novel mutations for infantile glaucoma and von Hippel's ulcer revisited
Kelberman D; Islam L; Jacques TS; Russell-Eggitt I; Bitner-Glindzicz M; Khaw PT; Nischal KK; Sowden JC
Ophthalmology 2011; 118: 1865-1873
47830 Confirmation and further mapping of the GLC3C locus in primary congenital glaucoma
Chen X; Chen Y; Wang L; Jiang D; Wang W; Xia M; Yu L; Sun X
Front Biosci 2011; 17: 2052-2059
48407 Overview of Cytochrome P450 1B1 gene mutations in patients with primary congenital glaucoma
Li N; Zhou Y; Du L; Wei M; Chen X
Experimental Eye Research 2011; 93: 572-579
47788 Circumferential trabeculotomy with an illuminated microcatheter in congenital glaucomas
Girkin CA; Marchase N; Cogen MS
Journal of Glaucoma 2011;
