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Journal Abstract Search


135 related items for PubMed ID: 12843897

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  • 2. Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1.
    Richards AJ, McNinch A, Martin H, Oakhill K, Rai H, Waller S, Treacy B, Whittaker J, Meredith S, Poulson A, Snead MP.
    Hum Mutat; 2010 Jun; 31(6):E1461-71. PubMed ID: 20513134
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  • 7. Ultrastructure of vitreomacular traction syndrome associated with persistent hyaloid artery.
    Gandorfer A, Rohleder M, Charteris D, Kampik A, Luthert P.
    Eye (Lond); 2005 Mar; 19(3):333-6. PubMed ID: 15258604
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  • 11. Vitreous veils and radial lattice in Marshall syndrome.
    Brubaker JW, Mohney BG, Pulido JS, Babovic-Vuksanovic D.
    Ophthalmic Genet; 2008 Dec; 29(4):184-5. PubMed ID: 19005991
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  • 12. Time course of posterior vitreous detachment in the second eye.
    Hikichi T.
    Curr Opin Ophthalmol; 2007 May; 18(3):224-7. PubMed ID: 17435430
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  • 19. Hereditary vitreopathy.
    Snead MP.
    Eye (Lond); 1996 May; 10 ( Pt 6)():653-63. PubMed ID: 9091360
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  • 20. Analysis of the vitreous membrane in a case of type 1 Stickler syndrome.
    Yokoi T, Koide R, Matsuoka K, Nakagawa A, Azuma N.
    Graefes Arch Clin Exp Ophthalmol; 2009 May; 247(5):715-8. PubMed ID: 19089441
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