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Ophthalmic Genetics|November 12, 1998
Characterization of antibody against the N-terminus of RDS/peripherinR Y Kim, M A Bedolli, J GoodarziOphthalmic Genetics|December 1, 1996
Pigmented ocular fundus lesions and APC mutations in familial adenomatous polyposisE I Traboulsi, J Apostolides, F M Giardiello, et al.Ophthalmic Genetics|September 1, 1996
G106R rhodopsin mutation is also present in Spanish ADRP patientsC Ayuso, C Reig, B Garcia-Sandoval, et al.Ophthalmic Genetics|June 1, 1996
Familial exudative vitreoretinopathy linked to D11S533 in a large Asian family with consanguinityS M Price, N Periam, A Humphries, et al.Ophthalmic Genetics|June 1, 1996
Bilateral epiretinal membranes: a new finding in Hunter syndromeA S Narita, I Russell-EggittOphthalmic Genetics|May 20, 2008
The D144E substitution in the VSX1 gene: a non-pathogenic variant or a disease causing mutation?Pras Eran, Abu Almogit, Zadok David, et al.Ophthalmic Genetics|May 20, 2008
Corneal opacities in the Hallermann-Streiff syndromeFrançoise M Roulez, Josée Schuil, Françoise M MeireOphthalmic Genetics|May 20, 2008
A phenotypic variant of Knobloch syndromeTheresa Anne Williams, Graham R Kirkby, Denise Williams, et al.Ophthalmic Genetics|March 26, 2008
Congential fibrosis of the extraocular muscles type I (CFEOM1) on the Arabian PeninsulaArif O Khan, Dania S Khalil, Nada A Al-TassanOphthalmic Genetics|March 26, 2008
Blepharophimosis-ptosis-epicanthus inversus syndrome in a girl with chromosome translocation t(2;3)(q33;q23)Andreas Tzschach, Christina Kelbova, Sabine Weidensee, et al.Pageof 185