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Ophthalmic Genetics|September 27, 2007
An unusual presentation of macular corneal dystrophy associated with uniparental isodisomy and a novel Leu173Pro mutationVivek S Yellore, Baris Sonmez, Michael C Chen, et al.Ophthalmic Genetics|October 20, 2006
Genetic evaluation to establish the diagnosis of X-linked familial exudative vitreoretinopathyKimberly A Drenser, Wendy Dailey, Antonio Capone, et al.Ophthalmic Genetics|October 20, 2006
Familial blepharophimosis-like syndrome with esotropia, uveal coloboma, and short statureArif O Khan, Syed K Alam, Mohammed Aldahmesh, et al.Ophthalmic Genetics|October 20, 2006
Corneal ectasia and hydrops in a patient with autosomal recessive cornea planaArif O Khan, Mohammed Aldahmesh, Brian MeyerOphthalmic Genetics|June 7, 2006
Scanning the ocular albinism 1 (OA1) gene for polymorphisms in congenital nystagmus by DHPLCGeorgina B Sallmann, Paula J Bray, Sophie Rogers, et al.Ophthalmic Genetics|June 7, 2006
Hunter syndrome (MPS II-B): a report of bilateral vitreous floaters and maculopathyMonique A AnawisOphthalmic Genetics|July 17, 2004
Genetic analysis of an Indian family with members affected with juvenile-onset primary open-angle glaucomaM Markandaya, T K Ramesh, V Selvaraju, et al.Ophthalmic Genetics|September 17, 2004
Autosomal dominant familial exudative vitreoretinopathy in two Japanese families with FZD4 mutations (H69Y and C181R)Satoshi Omoto, Takaaki Hayashi, Kenji Kitahara, et al.Ophthalmic Genetics|September 17, 2004
Rab escort protein 1 (REP1) in intracellular traffic: a functional and pathophysiological overviewMarkus Preising, Carmen AyusoPageof 185