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Journal Abstract Search

266 related items for PubMed ID: 20346889

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  • 2. [Retinitis pigmentosa--clinical and genetic aspects with low vision].
    Bogdănici C, Rusu C, Moţoc I, Crăşmaru C.
    Oftalmologia; 2008; 52(2):64-71. PubMed ID: 19065917
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  • 5. Concentric retinitis pigmentosa: clinicopathologic correlations.
    Milam AH, De Castro EB, Smith JE, Tang WX, John SK, Gorin MB, Stone EM, Aguirre GD, Jacobson SG.
    Exp Eye Res; 2001 Oct; 73(4):493-508. PubMed ID: 11825021
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  • 11. Screen of the IMPDH1 gene among patients with dominant retinitis pigmentosa and clinical features associated with the most common mutation, Asp226Asn.
    Wada Y, Sandberg MA, McGee TL, Stillberger MA, Berson EL, Dryja TP.
    Invest Ophthalmol Vis Sci; 2005 May; 46(5):1735-41. PubMed ID: 15851576
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  • 13. Mutations in the pre-mRNA splicing gene, PRPF31, in Japanese families with autosomal dominant retinitis pigmentosa.
    Sato H, Wada Y, Itabashi T, Nakamura M, Kawamura M, Tamai M.
    Am J Ophthalmol; 2005 Sep; 140(3):537-40. PubMed ID: 16139010
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  • 15. Ser186Pro mutation of RHO gene in a Spanish autosomal dominant retinitis pigmentosa (ADRP) family.
    Trujillo MJ, Garcia-Sandoval B, Lorda-Sanchez I, Gimenez A, Sanz R, Rodriguez de Alba M, Gonzalez-Gonzalez MC, Ibañez A, Ramos C, Ayuso C.
    Ophthalmic Genet; 2000 Dec; 21(4):251-6. PubMed ID: 11135497
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  • 16. Low incidence of retinitis pigmentosa among heterozygous carriers of a specific rhodopsin splice site mutation.
    Rosenfeld PJ, Hahn LB, Sandberg MA, Dryja TP, Berson EL.
    Invest Ophthalmol Vis Sci; 1995 Oct; 36(11):2186-92. PubMed ID: 7558711
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