Clinical study of a large family with autosomal dominant progressive cone degeneration.

[1]  K. Gehrs,et al.  Mapping of autosomal dominant cone degeneration to chromosome 17p. , 1996, American journal of ophthalmology.

[2]  P. Humphries,et al.  Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked family. , 1992, Human molecular genetics.

[3]  J. Oosterhuis,et al.  Late onset dominant cone dystrophy with early blue cone involvement. , 1992, Journal of medical genetics.

[4]  H. Fledelius,et al.  Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211. , 1991, American journal of medical genetics.

[5]  M. Marmor,et al.  Standard for Clinical Electroretinography: International Standardization Committee , 1989 .

[6]  R. Carr,et al.  Progressive peripheral cone dysfunction. , 1988, American journal of ophthalmology.

[7]  D. Archer,et al.  Retinal ultrastructural findings in cone degeneration. , 1988, American journal of ophthalmology.

[8]  R. Weleber,et al.  Normal α-L-Fucosidase and Other Lysosomal Enzyme Activities in Progressive Cone Dystrophy , 1988 .

[9]  R. Carr,et al.  Progressive cone dystrophy. , 1987, Transactions of the American Ophthalmological Society.

[10]  M. Warburg,et al.  Retinal cone dysfunction and mental retardation associated with a de novo balanced translocation 1;6(q44;q27). , 1986, Ophthalmic paediatrics and genetics.

[11]  G. Fish,et al.  A comparison of visual function tests in eyes with maculopathy. , 1986, Ophthalmology.

[12]  G. Fishman,et al.  Supernormal scotopic ERG in cone dystrophy. , 1984, The British journal of ophthalmology.

[13]  P. Gouras,et al.  Cone dystrophy, nyctalopia, and supernormal rod responses. A new retinal degeneration. , 1983, Archives of ophthalmology.

[14]  M. Sandberg,et al.  Foveal and parafoveal cone electroretinograms in juvenile macular degeneration , 1983 .

[15]  G. Fishman,et al.  Visual improvements with red-tinted glasses in a patient with cone dystrophy. , 1982, Archives of ophthalmology.

[16]  S. Jacobson,et al.  Foveal cone electroretinograms in retinitis pigmentosa and juvenile maular degeneration. , 1979, American journal of ophthalmology.

[17]  R. Blach,et al.  Bull's eye maculopathy with early cone degeneration. , 1977, The British journal of ophthalmology.

[18]  J. Pearlman,et al.  Cone dystrophy with dominant inheritance. , 1974, American journal of ophthalmology.

[19]  R. Schachar,et al.  Use of miotics in patients with cone degenerations. , 1973, American journal of ophthalmology.

[20]  A. Deutman,et al.  Dominant macular degenerations. The cone dystrophies. , 1972, American journal of ophthalmology.

[21]  P. Gouras,et al.  Progressive cone degeneration, dominantly inherited. , 1968, Archives of ophthalmology.

[22]  H. Ripps,et al.  CONE DYSFUNCTION SYNDROMES. , 1963, Archives of ophthalmology.

[23]  K. N. Ogle,et al.  Some physiologic considerations of hereditary mascular degeneration. , 1956, American journal of ophthalmology.