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Ophthalmic Genetics|September 4, 2008
The frequency of the H402 allele of CFH and its involvement with age-related maculopathy in an aged Black African Xhosa populationAri Ziskind, Soraya Bardien, Lize van der Merwe, et al.Ophthalmic Genetics|September 4, 2008
PAX6 analysis of two unrelated families from the Arabian Peninsula with classic hereditary aniridiaArif O Khan, Mohammad A AldahmeshOphthalmic Genetics|May 11, 2010
Characterization of Ca2+ signalling in postnatal mouse retinal ganglion cells: involvement of OPA1 in Ca2+ clearanceGovindan Dayanithi, Murielle Chen-Kuo-Chang, Cedric Viero, et al.Ophthalmic Genetics|May 11, 2010
A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutationAntonella Fabretto, Alison Shardlow, Flavio Faletra, et al.Ophthalmic Genetics|January 28, 2009
Macular dysfunction and morphology in spinocerebellar ataxia type 7 (SCA 7)Therése Hugosson, Lotta Gränse, Vesna Ponjavic, et al.Ophthalmic Genetics|January 28, 2009
The effect of therapy refusal against medical advice in retinoblastoma patients in a setting where treatment delays are commonRita S Sitorus, Annette C Moll, Setiowati Suhardjono, et al.Ophthalmic Genetics|January 28, 2009
Congenital alacrima in a patient with blepharophimosis syndromeGeetha K Athappilly, Rebecca Sands BravermanOphthalmic Genetics|April 18, 2009
Natural history of phenotypic changes in Stargardt macular dystrophySaloni Walia, Gerald A FishmanOphthalmic Genetics|April 18, 2009
Flecked-retina syndromesSaloni Walia, Gerald A Fishman, Rashmi KapurOphthalmic Genetics|April 18, 2009
Congenital fibrosis of the extraocular muscles type 1, distinctive conjunctival changes and intrapapillary disc colobomataMaree P Flaherty, Chandra Balachandran, Robyn Jamieson, et al.Pageof 185