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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

115 related items for PubMed ID: 519897

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  • 25. Autosomal recessive retinitis pigmentosa in a Pakistani family mapped to CNGA1 with identification of a novel mutation.
    Zhang Q, Zulfiqar F, Riazuddin SA, Xiao X, Ahmad Z, Riazuddin S, Hejtmancik JF.
    Mol Vis; 2004 Nov 17; 10():884-9. PubMed ID: 15570217
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  • 29. Mutation screening of 299 Spanish families with retinal dystrophies by Leber congenital amaurosis genotyping microarray.
    Vallespin E, Cantalapiedra D, Riveiro-Alvarez R, Wilke R, Aguirre-Lamban J, Avila-Fernandez A, Lopez-Martinez MA, Gimenez A, Trujillo-Tiebas MJ, Ramos C, Ayuso C.
    Invest Ophthalmol Vis Sci; 2007 Dec 17; 48(12):5653-61. PubMed ID: 18055816
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  • 33. Autosomal recessive retinitis pigmentosa is associated with mutations in RP1 in three consanguineous Pakistani families.
    Riazuddin SA, Zulfiqar F, Zhang Q, Sergeev YV, Qazi ZA, Husnain T, Caruso R, Riazuddin S, Sieving PA, Hejtmancik JF.
    Invest Ophthalmol Vis Sci; 2005 Jul 17; 46(7):2264-70. PubMed ID: 15980210
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  • 36. Retinitis pigmentosa, autosomal recessive type: three kindreds.
    Schleutermann D, Pierce E, Cantolino SJ, Naidoff M.
    Birth Defects Orig Artic Ser; 1971 Mar 17; 7(3):180-2. PubMed ID: 5173138
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  • 40. Attitudes of people with inherited retinal conditions toward gene editing technology.
    Hoffman-Andrews L, Mazzoni R, Pacione M, Garland-Thomson R, Ormond KE.
    Mol Genet Genomic Med; 2019 Jul 17; 7(7):e00803. PubMed ID: 31190471
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