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Journal Abstract Search

182 related items for PubMed ID: 7952338

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  • 4. Compound heterozygous RDH5 mutations in familial fleck retina with night blindness.
    Hayashi T, Goto-Omoto S, Takeuchi T, Gekka T, Ueoka Y, Kitahara K.
    Acta Ophthalmol Scand; 2006 Apr; 84(2):254-8. PubMed ID: 16637847
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  • 6. Flecked-retina syndromes.
    Walia S, Fishman GA, Kapur R.
    Ophthalmic Genet; 2009 Jun; 30(2):69-75. PubMed ID: 19373677
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  • 7. Atypical retinitis pigmentosa.
    O'Connor PR, John ME, Lawwill T, Vancader TC.
    Ann Ophthalmol; 1974 Aug; 6(8):824-6. PubMed ID: 4547147
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  • 9. A case of sectorial benign flecked retina.
    Tsuchiya T, Kato M, Tomita N, Koide K, Hata N, Sato M, Hotta Y, Ueno M, Nakamura M, Miyake Y.
    Jpn J Ophthalmol; 2004 Aug; 48(1):72-4. PubMed ID: 14767656
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  • 12. [Macular dystrophies].
    Souied E, Kaplan J, Coscas G, Soubrane G.
    J Fr Ophtalmol; 2003 Sep; 26(7):743-62. PubMed ID: 13130265
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  • 17. Novel mutation in RLBP1 gene in a Japanese patient with retinitis punctata albescens.
    Nakamura M, Lin J, Ito Y, Miyake Y.
    Am J Ophthalmol; 2005 Jun; 139(6):1133-5. PubMed ID: 15953459
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  • 18. The differential diagnosis of crystals in the retina.
    Nadim F, Walid H, Adib J.
    Int Ophthalmol; 2001 Jun; 24(3):113-21. PubMed ID: 12498506
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  • 20. Mutations in the gene encoding 11-cis retinol dehydrogenase cause delayed dark adaptation and fundus albipunctatus.
    Yamamoto H, Simon A, Eriksson U, Harris E, Berson EL, Dryja TP.
    Nat Genet; 1999 Jun; 22(2):188-91. PubMed ID: 10369264
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