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    Results: 1 to 20 of 99

    1.

    Mapping a new genetic locus for X linked retinitis pigmentosa to Xq28.

    Melamud A, Shen GQ, Chung D, Xi Q, Simpson E, Li L, Peachey NS, Zegarra H, Hagstrom SA, Wang QK, Traboulsi EI.

    J Med Genet. 2006 Jun;43(6):e27.PMID: 16740911 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    Clinical expression of X-linked retinitis pigmentosa in a Swedish family with the RP2 genotype.

    Ponjavic V, Andréasson S, Abrahamson M, Ehinger B, Gieser L, Fujita R, Swaroop A.

    Ophthalmic Genet. 1998 Dec;19(4):187-96.PMID: 9895243 [PubMed - indexed for MEDLINE]Related articles

    3.

    Novel RPGR mutations with distinct retinitis pigmentosa phenotypes in French-Canadian families.

    Koenekoop RK, Loyer M, Hand CK, Al Mahdi H, Dembinska O, Beneish R, Racine J, Rouleau GA.

    Am J Ophthalmol. 2003 Oct;136(4):678-87.PMID: 14516808 [PubMed - indexed for MEDLINE]Related articles

    4.

    X-linked high myopia associated with cone dysfunction.

    Young TL, Deeb SS, Ronan SM, Dewan AT, Alvear AB, Scavello GS, Paluru PC, Brott MS, Hayashi T, Holleschau AM, Benegas N, Schwartz M, Atwood LD, Oetting WS, Rosenberg T, Motulsky AG, King RA.

    Arch Ophthalmol. 2004 Jun;122(6):897-908.PMID: 15197065 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Evidence for a new locus for X-linked retinitis pigmentosa (RP23).

    Hardcastle AJ, Thiselton DL, Zito I, Ebenezer N, Mah TS, Gorin MB, Bhattacharya SS.

    Invest Ophthalmol Vis Sci. 2000 Jul;41(8):2080-6.PMID: 10892847 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    Phenotype in two families with RP3 associated with RPGR mutations.

    Lorenz B, Andrassi M, Kretschmann U.

    Ophthalmic Genet. 2003 Jun;24(2):89-101.PMID: 12789573 [PubMed - indexed for MEDLINE]Related articles

    7.

    Disease expression in X-linked retinitis pigmentosa caused by a putative null mutation in the RPGR gene.

    Jacobson SG, Buraczynska M, Milam AH, Chen C, Järvaläinen M, Fujita R, Wu W, Huang Y, Cideciyan AV, Swaroop A.

    Invest Ophthalmol Vis Sci. 1997 Sep;38(10):1983-97.PMID: 9331262 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    X-linked dominant cone-rod degeneration: linkage mapping of a new locus for retinitis pigmentosa (RP 15) to Xp22.13-p22.11.

    McGuire RE, Sullivan LS, Blanton SH, Church MW, Heckenlively JR, Daiger SP.

    Am J Hum Genet. 1995 Jul;57(1):87-94.PMID: 7611300 [PubMed - indexed for MEDLINE]Related articlesFree article

    9.

    X-linked retinitis pigmentosa in two families with a missense mutation in the RPGR gene and putative change of glycine to valine at codon 60.

    Fishman GA, Grover S, Jacobson SG, Alexander KR, Derlacki DJ, Wu W, Buraczynska M, Swaroop A.

    Ophthalmology. 1998 Dec;105(12):2286-96.PMID: 9855162 [PubMed - indexed for MEDLINE]Related articles

    10.

    Confirmation of linkage and refinement of the RP28 locus for autosomal recessive retinitis pigmentosa on chromosome 2p14-p15 in an Indian family.

    Kumar A, Shetty J, Kumar B, Blanton SH.

    Mol Vis. 2004 Jun 15;10:399-402.PMID: 15215745 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    A novel locus for X-linked retinitis pigmentosa.

    Tong Z, Yang Z, Meyer JJ, McInnes AW, Xue L, Azimi AM, Baird J, Zhao Y, Pearson E, Wang C, Chen Y, Zhang K.

    Ann Acad Med Singapore. 2006 Jul;35(7):476-8.PMID: 16902723 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene.

    Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Yasmeen A, Rogan PK, Caruso R, Sieving PA, Riazuddin S, Hejtmancik JF.

    Mol Vis. 2005 Nov 14;11:977-85.PMID: 16319817 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    A new 2-base pair deletion in the RPGR gene in a black family with X-linked retinitis pigmentosa.

    Fishman GA, Grover S, Buraczynska M, Wu W, Swaroop A.

    Arch Ophthalmol. 1998 Feb;116(2):213-8.PMID: 9488274 [PubMed - indexed for MEDLINE]Related articlesFree article

    14.

    Variable expressivity in a Japanese family with autosomal dominant retinitis pigmentosa closely linked to chromosome 19q.

    Nakazawa M, Xu S, Gal A, Wada Y, Tamai M.

    Arch Ophthalmol. 1996 Mar;114(3):318-22.PMID: 8600893 [PubMed - indexed for MEDLINE]Related articles

    15.

    Clinical and genetic studies of an autosomal dominant cone-rod dystrophy with features of Stargardt disease.

    Kniazeva MF, Chiang MF, Cutting GR, Zack DJ, Han M, Zhang K.

    Ophthalmic Genet. 1999 Jun;20(2):71-81.PMID: 10420191 [PubMed - indexed for MEDLINE]Related articles

    16.

    Localization of the gene for X-linked recessive type of retinitis pigmentosa (XLRP) to Xp21 by linkage analysis.

    Musarella MA, Burghes A, Anson-Cartwright L, Mahtani MM, Argonza R, Tsui LC, Worton R.

    Am J Hum Genet. 1988 Oct;43(4):484-94.PMID: 2902787 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Clinical and electroretinographic findings of female carriers and affected males in a progressive X-linked cone-rod dystrophy (COD-1) pedigree.

    Brown J Jr, Kimura AE, Gorin MB.

    Ophthalmology. 2000 Jun;107(6):1104-10. Erratum in: Ophthalmology 2000 Aug;107(8):1440. PMID: 10857830 [PubMed - indexed for MEDLINE]Related articles

    18.

    Electrophysiologic and phenotypic features of an autosomal cone-rod dystrophy caused by a novel CRX mutation.

    Lines MA, Hébert M, McTaggart KE, Flynn SJ, Tennant MT, MacDonald IM.

    Ophthalmology. 2002 Oct;109(10):1862-70.PMID: 12359607 [PubMed - indexed for MEDLINE]Related articles

    19.

    Phenotypic expression of autosomal dominant retinitis pigmentosa in a Swedish family expressing a Phe-211-Leu variant of peripherin/RDS.

    Ekström U, Ponjavic V, Abrahamson M, Nilsson-Ehle P, Andrëasson S, Stenström I, Ehinger B.

    Ophthalmic Genet. 1998 Mar;19(1):27-37.PMID: 9587927 [PubMed - indexed for MEDLINE]Related articles

    20.

    A novel locus (RP24) for X-linked retinitis pigmentosa maps to Xq26-27.

    Gieser L, Fujita R, Göring HH, Ott J, Hoffman DR, Cideciyan AV, Birch DG, Jacobson SG, Swaroop A.

    Am J Hum Genet. 1998 Nov;63(5):1439-47.PMID: 9792872 [PubMed - indexed for MEDLINE]Related articlesFree article

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