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Journal Abstract Search

125 related items for PubMed ID: 7748141

  • 1. 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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  • 2. Autosomal dominant rhegmatogenous retinal detachment associated with an Arg453Ter mutation in the COL2A1 gene.
    Go SL, Maugeri A, Mulder JJ, van Driel MA, Cremers FP, Hoyng CB.
    Invest Ophthalmol Vis Sci; 2003 Sep; 44(9):4035-43. PubMed ID: 12939326
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  • 11. 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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  • 14. 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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  • 15. Snowflake vitreoretinal degeneration: follow-up of the original family.
    Lee MM, Ritter R, Hirose T, Vu CD, Edwards AO.
    Ophthalmology; 2003 Dec; 110(12):2418-26. PubMed ID: 14644728
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  • 16. Reduced penetrance in a large Caucasian pedigree with Stickler syndrome.
    Tompson SW, Johnson C, Abbott D, Bakall B, Soler V, Yanovitch TL, Whisenhunt KN, Klemm T, Rozen S, Stone EM, Johnson M, Young TL.
    Ophthalmic Genet; 2017 Dec; 38(1):43-50. PubMed ID: 28095098
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  • 19. A Stickler syndrome gene is linked to chromosome 6 near the COL11A2 gene.
    Brunner HG, van Beersum SE, Warman ML, Olsen BR, Ropers HH, Mariman EC.
    Hum Mol Genet; 1994 Sep; 3(9):1561-4. PubMed ID: 7833911
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  • 20. Genetic linkage of autosomal dominant neovascular inflammatory vitreoretinopathy to chromosome 11q13.
    Stone EM, Kimura AE, Folk JC, Bennett SR, Nichols BE, Streb LM, Sheffield VC.
    Hum Mol Genet; 1992 Dec; 1(9):685-9. PubMed ID: 1284594
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