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9.1.1 Congenital glaucoma, Buphthalmos (9)
Showing records 1 to 9
Display all abstracts in classification 9.1.1 Congenital glaucoma, Buphthalmos
Search within classification 9.1.1 Congenital glaucoma, Buphthalmos28241 Reconstructing the Indian origin and dispersal of the european Roma: A maternal genetic perspective
Mendizabal I; Valente C; Gusmao A; Alves C; Gomes V; Goios A; Parson W; Calafell F; Alvarez L; Amorim A
PLoS ONE 2011; 6: 15988
28006 Novel GLIS3 mutations demonstrate an extended multisystem phenotype
Dimitri P; Warner JT; Minton JAL; Patch AM; Ellard S; Hattersley AT; Barr S; Hawkes D; Wales JK; Gregory JW
European Journal of Endocrinology 2011; 164: 437-443
27781 Expanding the Spectrum of FOXC1 and PITX2 Mutations and Copy Number Changes in Patients with Anterior Segment Malformations
D'haene B; Meire F; Claerhout I; Kroes HY; Plomp A; Arens YH; de Ravel T; Casteels I; De Jaegere S; Hooghe S
Investigative Ophthalmology and Visual Science 2011; 52: 324-333
27796 Genotype/phenotype correlation in primary congenital glaucoma patients from different ethnic groups of the israeli population
Geyer O; Wolf A; Levinger E; Harari-Shacham A; Walton DS; Shochat C; Korem S; Bercovich D
American Journal of Ophthalmology 2011; 151: 263-271
27918 Outcomes of goniotomy for primary congenital glaucoma in East Africa
Bowman RJC; Dickerson M; Mwende J; Khaw PT
Ophthalmology 2011; 118: 236-240
27920 Surgical results in the management of advanced primary congenital glaucoma in a rural pediatric population
Ben-Zion I; Tomkins O; Moore DB; Helveston EM
Ophthalmology 2011; 118: 231-235
28023 Combined trabeculotomy and trabeculectomy: Outcome for primary congenital glaucoma in a West African population
Essuman VA; Braimah IZ; Ndanu TA; Ntim-Amponsah CT
Eye 2011; 25: 77-83
27780 Anophthalmos, Microphthalmos, and Typical Coloboma in the United Kingdom: A Prospective Study of Incidence and Risk
Shah SP; Taylor AE; Sowden JC; Ragge NK; Russell-Eggitt I; Rahi JS; Gilbert CE
Investigative Ophthalmology and Visual Science 2011; 52: 558-564
27990 Genome-wide homozygosity mapping and next generation sequencing indentifies SAMHD1 mutations in a novel variant of Aicardi-Goutieres syndrome
Du Moulin M; Thiele H; Barczyk K; George C; Frosch M; Schwindt W; Roth J; Nurnberg P; Rutsch F
European Journal of Pediatrics 2010; 169: 380-381