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Journal Abstract Search

131 related items for PubMed ID: 10333105

  • 1. Wagner vitreoretinal degeneration with genetic linkage refinement on chromosome 5q13-q14.
    Zech JC, Morlé L, Vincent P, Alloisio N, Bozon M, Gonnet C, Milazzo S, Grange JD, Trepsat C, Godet J, Plauchu H.
    Graefes Arch Clin Exp Ophthalmol; 1999 May; 237(5):387-93. PubMed ID: 10333105
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  • 6. Posterior chorioretinal atrophy and vitreous phenotype in a family with Stickler syndrome from a mutation in the COL2A1 gene.
    Vu CD, Brown J, Körkkö J, Ritter R, Edwards AO.
    Ophthalmology; 2003 Jan; 110(1):70-7. PubMed ID: 12511349
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  • 7. Wagner vitreoretinal degeneration. Follow-up of the original pedigree.
    Graemiger RA, Niemeyer G, Schneeberger SA, Messmer EP.
    Ophthalmology; 1995 Dec; 102(12):1830-9. PubMed ID: 9098284
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  • 8. Identification of a novel splice site mutation of the CSPG2 gene in a Japanese family with Wagner syndrome.
    Miyamoto T, Inoue H, Sakamoto Y, Kudo E, Naito T, Mikawa T, Mikawa Y, Isashiki Y, Osabe D, Shinohara S, Shiota H, Itakura M.
    Invest Ophthalmol Vis Sci; 2005 Aug; 46(8):2726-35. PubMed ID: 16043844
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  • 12. Clinical description and exclusion of candidate genes in a novel autosomal recessively inherited vitreoretinal dystrophy.
    Sarra GM, Weigell-Weber M, Kotzot D, Niemeyer G, Messmer E, Hergersberg M.
    Arch Ophthalmol; 2003 Aug; 121(8):1109-16. PubMed ID: 12912687
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  • 14. Mutational hot spot potential of a novel base pair mutation of the CSPG2 gene in a family with Wagner syndrome.
    Ronan SM, Tran-Viet KN, Burner EL, Metlapally R, Toth CA, Young TL.
    Arch Ophthalmol; 2009 Nov; 127(11):1511-9. PubMed ID: 19901218
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  • 18. Wagner's hereditary vitreoretinal degeneration.
    Manning LM.
    Aust J Ophthalmol; 1980 Feb; 8(1):29-33. PubMed ID: 7387542
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  • 19. Genetic linkage of Wagner disease and erosive vitreoretinopathy to chromosome 5q13-14.
    Brown DM, Graemiger RA, Hergersberg M, Schinzel A, Messmer EP, Niemeyer G, Schneeberger SA, Streb LM, Taylor CM, Kimura AE.
    Arch Ophthalmol; 1995 May; 113(5):671-5. PubMed ID: 7748141
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  • 20. Dominant late-onset retinal degeneration with regional variation of sub-retinal pigment epithelium deposits, retinal function, and photoreceptor degeneration.
    Milam AH, Curcio CA, Cideciyan AV, Saxena S, John SK, Kruth HS, Malek G, Heckenlively JR, Weleber RG, Jacobson SG.
    Ophthalmology; 2000 Dec; 107(12):2256-66. PubMed ID: 11097607
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