Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.

[1]  P. Humphries,et al.  Retinitis pigmentosa: genetic mapping in X‐linked and autosomal forms of the disease , 1990, Clinical genetics.

[2]  D. McConnell,et al.  Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21. , 1989, Genomics.

[3]  D. McConnell,et al.  Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locus. , 1989, American journal of human genetics.

[4]  D. McConnell,et al.  Linkage analysis of human chromosome 4: exclusion of autosomal dominant retinitis pigmentosa (ADRP) and detection of new linkage groups. , 1989, Cytogenetics and cell genetics.

[5]  J Attwood,et al.  A computer program to make linkage analysis with liped and linkage easier to perform and less prone to input errors , 1988, Annals of human genetics.

[6]  P. A. Peterson,et al.  Human cellular retinol-binding protein gene organization and chromosomal location. , 1988, European journal of biochemistry.

[7]  M. Daly,et al.  A genetic linkage map of the human genome , 1987, Cell.

[8]  P. Humphries,et al.  Observations on the structure of two human 7SK pseudogenes and on homologous transcripts in vertebrate species. , 1987, The Biochemical journal.

[9]  T. Mohandas,et al.  The cellular retinol binding protein II gene. Sequence analysis of the rat gene, chromosomal localization in mice and humans, and documentation of its close linkage to the cellular retinol binding protein gene. , 1987, The Journal of biological chemistry.

[10]  S. Daiger,et al.  DNA linkage studies of degenerative retinal diseases. , 1987, Progress in clinical and biological research.

[11]  J. Grøndahl Tapeto-retinal degeneration in four Norwegian counties, II. Diagnostic evaluation of 407 relatives and genetic evaluation of 87 families. , 2008, Clinical genetics.

[12]  T. Beaty,et al.  Problems in detecting etiological heterogeneity in genetic disease illustrated with retinitis pigmentosa. , 1986, American journal of medical genetics.

[13]  J. Nathans,et al.  Molecular genetics of inherited variation in human color vision. , 1986, Science.

[14]  S. Crews,et al.  A study of retinitis pigmentosa in the City of Birmingham. II Clinical and genetic heterogeneity. , 1984, Journal of medical genetics.

[15]  M. Rocchi,et al.  Mapping of human cellular retinol-binding protein to chromosome 3. , 1986, Cytogenetics and cell genetics.

[16]  R. M. Carter,et al.  A clinical, psychophysical, and electroretinographic survey of patients with autosomal dominant retinitis pigmentosa. , 1985, The British journal of ophthalmology.

[17]  G. Fishman,et al.  Autosomal dominantly inherited retinitis pigmentosa. Visual acuity loss by subtype. , 1985, Archives of ophthalmology.

[18]  S. Crews,et al.  A study of retinitis pigmentosa in the City of Birmingham. I Prevalence. , 1984, Journal of medical genetics.

[19]  J. Ott,et al.  Strategies for multilocus linkage analysis in humans. , 1984, Proceedings of the National Academy of Sciences of the United States of America.

[20]  E. Berson,et al.  Prevalence of retinitis pigmentosa in Maine. , 1984, American journal of ophthalmology.

[21]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[22]  C. M. Kemp,et al.  Visual pigment levels in retinitis pigmentosa. , 1983, Transactions of the ophthalmological societies of the United Kingdom.

[23]  G. Weinstein,et al.  Electroretinography and retinitis pigmentosa. No discrimination between genetic subtypes. , 1982, Archives of ophthalmology.

[24]  M. Spence,et al.  Linkage analysis of five pedigrees affected with typical autosomal dominant retinitis pigmentosa. , 1982, Journal of medical genetics.

[25]  M. Spence,et al.  Possible assignment of a dominant retinitis pigmentosa gene to chromosome 1. , 1982, Ophthalmic research.

[26]  J. Ott Estimation of the recombination fraction in human pedigrees: efficient computation of the likelihood for human linkage studies. , 1974, American journal of human genetics.

[27]  A. Rahi Retinol-binding protein (RBP) and pigmentary dystrophy of the retina. , 1972, The British journal of ophthalmology.