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Journal Abstract Search

171 related items for PubMed ID: 1929926

  • 1. Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosa.
    Fishman GA, Stone EM, Gilbert LD, Kenna P, Sheffield VC.
    Arch Ophthalmol; 1991 Oct; 109(10):1387-93. PubMed ID: 1929926
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  • 2. Ocular findings associated with rhodopsin gene codon 17 and codon 182 transition mutations in dominant retinitis pigmentosa.
    Fishman GA, Stone EM, Sheffield VC, Gilbert LD, Kimura AE.
    Arch Ophthalmol; 1992 Jan; 110(1):54-62. PubMed ID: 1731723
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  • 3. Ocular findings associated with a rhodopsin gene codon 106 mutation. Glycine-to-arginine change in autosomal dominant retinitis pigmentosa.
    Fishman GA, Stone EM, Gilbert LD, Sheffield VC.
    Arch Ophthalmol; 1992 May; 110(5):646-53. PubMed ID: 1580841
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  • 4. A new codon 15 rhodopsin gene mutation in autosomal dominant retinitis pigmentosa is associated with sectorial disease.
    Sullivan LJ, Makris GS, Dickinson P, Mulhall LE, Forrest S, Cotton RG, Loughnan MS.
    Arch Ophthalmol; 1993 Nov; 111(11):1512-7. PubMed ID: 8240107
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  • 5. Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.
    van den Born LI, van Schooneveld MJ, de Jong LA, Riemslag FC, de Jong PT, Gal A, Bleeker-Wagemakers EM.
    Ophthalmic Genet; 1994 Jun; 15(2):51-60. PubMed ID: 7850269
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  • 8. Ocular findings associated with rhodopsin gene codon 267 and codon 190 mutations in dominant retinitis pigmentosa.
    Fishman GA, Vandenburgh K, Stone EM, Gilbert LD, Alexander KR, Sheffield VC.
    Arch Ophthalmol; 1992 Nov; 110(11):1582-8. PubMed ID: 1444916
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  • 11. [Identification of Arg-135-Leu mutation in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa].
    Reig C, Antich J, Gean E, Dante Heredia C, Valverde D, Baiget M, Carballo M.
    Med Clin (Barc); 1996 Feb 17; 106(6):219-21. PubMed ID: 8667664
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  • 12. Clinical features of autosomal dominant retinitis pigmentosa with rhodopsin gene codon 17 mutation and retinal neovascularization in a Japanese patient.
    Hayakawa M, Hotta Y, Imai Y, Fujiki K, Nakamura A, Yanashima K, Kanai A.
    Am J Ophthalmol; 1993 Feb 15; 115(2):168-73. PubMed ID: 7679248
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  • 16. A six-generation family with autosomal dominant retinitis pigmentosa and a rhodopsin gene mutation (arginine-135-leucine).
    Andréasson S, Ehinger B, Abrahamson M, Fex G.
    Ophthalmic Paediatr Genet; 1992 Sep 15; 13(3):145-53. PubMed ID: 1484692
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  • 18. Clinical features of Japanese family with autosomal dominant retinitis pigmentosa caused by point mutation in codon 347 of rhodopsin gene.
    Shiono T, Hotta Y, Noro M, Sakuma T, Tamai M, Hayakawa M, Hashimoto T, Fujiki K, Kanai A, Nakajima A.
    Jpn J Ophthalmol; 1992 Sep 15; 36(1):69-75. PubMed ID: 1635298
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  • 20. Ocular findings in a form of retinitis pigmentosa with a rhodopsin gene defect.
    Berson EL.
    Trans Am Ophthalmol Soc; 1990 Sep 15; 88():355-88. PubMed ID: 2095030
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