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Ophthalmic Genetics|September 17, 2004
Evaluation of the ARMD1 locus on 1q25-31 in patients with age-related maculopathy: genetic variation in laminin genes and in exon 104 of HEMICENTIN-1M Hayashi, J E Merriam, C C W Klaver, et al.Ophthalmic Genetics|September 17, 2004
A novel KERA mutation associated with autosomal recessive cornea planaArif Khan, Amr Al-Saif, Marios KambourisOphthalmic Genetics|July 16, 2005
A discordant sib-pair linkage analysis of age-related macular degenerationSusan L Santangelo, Chen-Hsing Yen, Stephen Haddad, et al.Ophthalmic Genetics|July 16, 2005
X-linked infantile periodic alternating nystagmusRichard W Hertle, Dongsheng Yang, Kristopher Kelly, et al.Ophthalmic Genetics|September 21, 2016
Pharmacological approaches to restoring lens transparency: Real world applicationsCassandra Skinner, Virginia Miraldi UtzOphthalmic Genetics|February 10, 2010
Ophthalmologic abnormalities in a de novo terminal 6q deletionKhaled K Abu-Amero, Ali Hellani, Mustafa A Salih, et al.Ophthalmic Genetics|February 10, 2010
Does acute loss of vision in autosomal dominant optic atrophy occur early in childhood?Lisa S Kearns, Michael Forrest, Amy C Cohn, et al.Ophthalmic Genetics|February 10, 2010
Confirmation of ADAMTSL4 mutations for autosomal recessive isolated bilateral ectopia lentisV Bennouna Greene, C Stoetzel, V Pelletier, et al.Ophthalmic Genetics|August 2, 2018
CRX-linked macular dystrophy with intrafamilial variable expressivityKhaled Romdhane, Veronika Vaclavik, Daniel F Schorderet, et al.Ophthalmic Genetics|August 2, 2018
Familial non-syndromic macular pseudocoloboma secondary to homozygous CLDN19 mutationArif O Khan, Nisha Patel, Nicola G Ghazi, et al.Pageof 185