D. Y. Zhao

A homozygous PDE6B mutation in a family with autosomal recessive retinitis pigmentosa.

S. Jacobson, D. Farber, M. Danciger, 1996, Molecular vision.

Screening of the PDE6B gene in patients with autosomal dominant retinitis pigmentosa.

S. Jacobson, D. Farber, M. Danciger, 1996, Experimental Eye Research.

Mutations in the PDE6B gene in autosomal recessive retinitis pigmentosa.

S. Jacobson, J. Heckenlively, D. Farber, 1995, Genomics.

Screening of the gene encoding the alpha'-subunit of cone cGMP-PDE in patients with retinal degenerations.

S. Jacobson, G. Fishman, E. Stone, 1999, Investigative ophthalmology & visual science.

Exon screening of the genes encoding the beta- and gamma-subunits of cone transducin in patients with inherited retinal disease.

S. Jacobson, G. Fishman, J. Heckenlively, 1998, Molecular vision.

Choroidal melanoma in a patient with retinitis pigmentosa and Usher’s syndrome

C. Shields, J. Shields, K. Gündüz, 1998, The British journal of ophthalmology.