A. Frost

Autosomal dominant Stargardt-like macular dystrophy.

A. Edwards, E. Stone, L. Donoso, 2001, Survey of ophthalmology.

Autosomal dominant macular dystrophy in a large Canadian family.

V. Sheffield, L. Donoso, I. MacDonald, 2003, Canadian journal of ophthalmology. Journal canadien d'ophtalmologie.

X-linked retinoschisis: a clinical and molecular genetic review.

L. Donoso, T. Vrabec, W. Annesley, 2004, Survey of ophthalmology.

Identification of a stop codon mutation in exon 2 of the collagen 2A1 gene in a large stickler syndrome family.

A. Edwards, R. Ritter, L. Donoso, 2002, American journal of ophthalmology.

The role of inflammation in the pathogenesis of age-related macular degeneration.

Alston Callahan, L. Donoso, G. Hageman, 2006, Survey of ophthalmology.

X-linked retinoschisis: report of a family with a rare deletion in the XLRS1 gene.

L. Donoso, T. Vrabec, W. Annesley, 2003, American journal of ophthalmology.

Autosomal dominant Stargardt-like macular dystrophy: founder effect and reassessment of genetic heterogeneity.

A. Edwards, R. Ritter, E. Stone, 2001, Archives of ophthalmology.

X-LINKED RETINOSCHISIS: Novel Mutation in the Initiation Codon of the XLRS1 Gene in a Large Family

L. Donoso, T. Vrabec, J. Sassani, 2006, Retina.

Clinical variability of Stickler syndrome: role of exon 2 of the collagen COL2A1 gene.

A. Edwards, R. Ritter, L. Donoso, 2003, Survey of ophthalmology.

Autosomal dominant Stargardt-like macular dystrophy: identification of a new family with a mutation in the ELOVL4 gene.

A. Edwards, L. Donoso, T. Vrabec, 2003, American journal of ophthalmology.