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Ophthalmic Genetics|October 16, 1999
Genotype-phenotype correlation in X-linked retinitis pigmentosa 2 (RP2)T Rosenberg, U Schwahn, S Feil, et al.Ophthalmic Genetics|July 27, 1999
EEM syndrome: report of a family and results of a ten-year follow-upV Balarin Silva, A M Simões, A P Marques-de-FariaOphthalmic Genetics|July 27, 1999
1147 del A mutation in the arrestin gene in Japanese patients with Oguchi diseaseT Yamada, M Matsumoto, C Kadoi, et al.Ophthalmic Genetics|July 27, 1999
Retinal degeneration associated with ectopia lentisF Simonelli, G De Crecchio, F Testa, et al.Ophthalmic Genetics|July 23, 1999
Intraocular carboplatin concentrations following intravenous administration for human intraocular retinoblastomaD H Abramson, C M Frank, G L Chantada, et al.Ophthalmic Genetics|April 26, 2000
Familial occurrence of artefactual ocular hypertension from thick corneas and of primary open angle glaucoma in a French Canadian kindredA A Dohadwala, K F DamjiOphthalmic Genetics|January 5, 2000
Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophyY G Mashima, R G Weleber, N G Kennaway, et al.Ophthalmic Genetics|January 5, 2000
Iridocorneal adhesions in patients with the Marfan syndromeP J Arnold, M J Donohoe, M J Greenwald, et al.Ophthalmic Genetics|August 1, 2000
An unusual central retinal dystrophy associated with ichthyosis vulgarisO A Saatci, Z Ozbek, S Köse, et al.Ophthalmic Genetics|November 3, 2017
Analysis of the polymorphic variants of RAN and GEMIN3 genes and risk of Primary Open-Angle Glaucoma in the Polish populationMilena Molasy, Anna Walczak, Karolina Przybyłowska-Sygut, et al.Pageof 185