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Ophthalmic Genetics|March 28, 2003
Cataract in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD)I M Russell-Eggitt, J V Leonard, A M Lund, et al.Ophthalmic Genetics|June 6, 2003
Ophthalmic manifestations of congenital disorder of glycosylation type 1aHanne Jensen, Susanne Kjaergaard, Flemming Klie, et al.Ophthalmic Genetics|February 5, 2003
A pooled case-control study of the apolipoprotein E (APOE) gene in age-related maculopathySilke Schmidt, Caroline Klaver, Ann Saunders, et al.Ophthalmic Genetics|August 21, 2002
Clinical features of achromatopsia in Swedish patients with defined genotypesLouise Eksandh, Susanne Kohl, Bernd WissingerOphthalmic Genetics|August 21, 2002
Mutational analysis of the RB1 gene in Indian patients with retinoblastomaM Ata-ur-Rasheed, Geeta k Vemuganti, Santosh g Honavar, et al.Ophthalmic Genetics|July 18, 2003
Ocular manifestations in Fabry disease: a survey of 32 hemizygous male patientsChristophe Orssaud, Jean Dufier, Dominique GermainOphthalmic Genetics|July 18, 2003
Protein expression, genomic structure, and polymorphisms of oculomedinNagako Fujiwara, Toshihiko Matsuo, Hiroshi OhtsukiOphthalmic Genetics|July 18, 2003
Mutational analysis of the OA1 gene in ocular albinismOlivier Camand, Sandrine Boutboul, Laurence Arbogast, et al.Ophthalmic Genetics|November 14, 2019
Microphthalmos-anophthalmos-coloboma (MAC) spectrum in two brothers with Renpenning syndrome due to a truncating mutation in the polyglutamine tract binding protein 1 (PQBP1) geneMaha M Mameesh, Adila Al-Kindy, Majda Al-Yahyai, et al.Pageof 185