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301 related items for PubMed ID: 24529551

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  • 3. Abnormal cone structure in foveal schisis cavities in X-linked retinoschisis from mutations in exon 6 of the RS1 gene.
    Duncan JL, Ratnam K, Birch DG, Sundquist SM, Lucero AS, Zhang Y, Meltzer M, Smaoui N, Roorda A.
    Invest Ophthalmol Vis Sci; 2011 Dec 20; 52(13):9614-23. PubMed ID: 22110067
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  • 5. Clinical and genetic findings in Hungarian patients with X-linked juvenile retinoschisis.
    Lesch B, Szabó V, Kánya M, Somfai GM, Vámos R, Varsányi B, Pámer Z, Knézy K, Salacz G, Janáky M, Ferencz M, Hargitai J, Papp A, Farkas A.
    Mol Vis; 2008 Dec 20; 14():2321-32. PubMed ID: 19093009
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  • 7. Null retinoschisin-protein expression from an RS1 c354del1-ins18 mutation causing progressive and severe XLRS in a cross-sectional family study.
    Vijayasarathy C, Ziccardi L, Zeng Y, Smaoui N, Caruso RC, Sieving PA.
    Invest Ophthalmol Vis Sci; 2009 Nov 20; 50(11):5375-83. PubMed ID: 19474399
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  • 8. Clinical presentations of X-linked retinoschisis in Taiwanese patients confirmed with genetic sequencing.
    Wang NK, Liu L, Chen HM, Tsai S, Chang TC, Tsai TH, Yang CM, Chao AN, Chen KJ, Kao LY, Yeung L, Yeh LK, Hwang YS, Wu WC, Lai CC.
    Mol Vis; 2015 Nov 20; 21():487-501. PubMed ID: 25999676
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  • 11. A phenotype-genotype correlation study of X-linked retinoschisis.
    Vincent A, Robson AG, Neveu MM, Wright GA, Moore AT, Webster AR, Holder GE.
    Ophthalmology; 2013 Jul 20; 120(7):1454-64. PubMed ID: 23453514
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  • 14. Phenotypic Characteristics of a French Cohort of Patients with X-Linked Retinoschisis.
    Orès R, Mohand-Said S, Dhaenens CM, Antonio A, Zeitz C, Augstburger E, Andrieu C, Sahel JA, Audo I.
    Ophthalmology; 2018 Oct 20; 125(10):1587-1596. PubMed ID: 29739629
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  • 16. Genotypic and phenotypic diversity in X-linked retinoschisis: Findings from a South Indian patient cohort.
    Chowdhury S, Chermakani P, Baliga G, Anjanamurthy R, Sundaresan P.
    Indian J Ophthalmol; 2024 Jun 01; 72(6):902-911. PubMed ID: 38317323
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  • 17. Novel mutations of the RS1 gene in a cohort of Chinese families with X-linked retinoschisis.
    Chen J, Xu K, Zhang X, Pan Z, Dong B, Li Y.
    Mol Vis; 2014 Jun 01; 20():132-9. PubMed ID: 24505212
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  • 18. Four Japanese male patients with juvenile retinoschisis: only three have mutations in the RS1 gene.
    Hayashi T, Omoto S, Takeuchi T, Kozaki K, Ueoka Y, Kitahara K.
    Am J Ophthalmol; 2004 Nov 01; 138(5):788-98. PubMed ID: 15531314
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  • 19. Case report of an atypical early onset X-linked retinoschisis in monozygotic twins.
    Murro V, Caputo R, Bacci GM, Sodi A, Mucciolo DP, Bargiacchi S, Giglio SR, Virgili G, Rizzo S.
    BMC Ophthalmol; 2017 Feb 24; 17(1):19. PubMed ID: 28235399
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  • 20. Long-term 12 year follow-up of X-linked congenital retinoschisis.
    Kjellström S, Vijayasarathy C, Ponjavic V, Sieving PA, Andréasson S.
    Ophthalmic Genet; 2010 Sep 24; 31(3):114-25. PubMed ID: 20569020
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