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Journal Abstract Search

207 related items for PubMed ID: 6336261

  • 1. Congenital hereditary endothelial dystrophy.
    Collum LM, Lavin J, Mullaney J.
    Bull Soc Belge Ophtalmol; 1984; 211():1-5. PubMed ID: 6336261
    [No Abstract] [Full Text] [Related]

  • 2. Familial spinocerebellar degeneration with corneal dystrophy.
    Der Kaloustian VM, Jarudi NI, Khoury MJ, Afifi AK, Bahuth NB, Deeb ME, Shammas J, Mikati MA.
    Am J Med Genet; 1985 Feb; 20(2):325-39. PubMed ID: 3872072
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  • 4. [Groenouw I type dystrophy in its diffuse superficial form].
    Pouliquen Y, Dhermy P, Monteil C, Legras M.
    Bull Mem Soc Fr Ophtalmol; 1977 Feb; 89():327-35. PubMed ID: 305799
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  • 7. Microcystic corneal dystrophy.
    Laibson PR.
    Trans Am Ophthalmol Soc; 1976 Feb; 74():488-531. PubMed ID: 301322
    [No Abstract] [Full Text] [Related]

  • 8. Localization of the gene for autosomal recessive congenital hereditary endothelial dystrophy (CHED2) to chromosome 20 by homozygosity mapping.
    Hand CK, Harmon DL, Kennedy SM, FitzSimon JS, Collum LM, Parfrey NA.
    Genomics; 1999 Oct 01; 61(1):1-4. PubMed ID: 10512674
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  • 12. [A hitherto unknown subepithelial hereditary corneal dystrophy].
    Thiel HJ, Behnke H.
    Klin Monbl Augenheilkd; 1967 Oct 01; 150(6):862-74. PubMed ID: 5301630
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  • 14. Congenital hereditary corneal dystrophy--a histopathological report.
    Limaye SR, Kothare SN.
    Eye Ear Nose Throat Mon; 1972 Sep 01; 51(9):355-8. PubMed ID: 4538365
    [No Abstract] [Full Text] [Related]

  • 15. The histological and ultrastructural pathology of congenital hereditary corneal dystrophy: a case report.
    Kenyon KR, Maumenee AE.
    Invest Ophthalmol; 1968 Oct 01; 7(5):475-500. PubMed ID: 4234642
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  • 16. [Dominant hereditary early infantile progressive endothelial corneal dystrophy (horseshoe-shaped beginning variant of Schlichting's endothelial dystrophy)].
    Jaeger W, Sundmacher R, Witschel H, Stangl R.
    Buch Augenarzt; 1982 Oct 01; 88():108-15. PubMed ID: 6979374
    [No Abstract] [Full Text] [Related]

  • 17. [Congenital hereditary corneal endothelial dystrophy].
    Hinzpeter EN, Naumann G.
    Ber Zusammenkunft Dtsch Ophthalmol Ges; 1972 Oct 01; 71():585-91. PubMed ID: 4582034
    [No Abstract] [Full Text] [Related]

  • 18. Hereditary crystalline corneal dystrophy with an associated blood lipid disorder.
    Williams HP, Bron AJ, Tripathi RC, Garner A.
    Trans Ophthalmol Soc U K (1962); 1971 Oct 01; 91():531-41. PubMed ID: 5316991
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  • 19. [Familial corneal degeneration--type Reis-Bücklers (author's transl)].
    Dałkowska A, Pecoldowa K.
    Klin Oczna; 1981 Oct 01; 83(10-12):515-8. PubMed ID: 6980318
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  • 20. Severe corneal dystrophy phenotype caused by homozygous R124H keratoepithelin mutations.
    Okada M, Yamamoto S, Inoue Y, Watanabe H, Maeda N, Shimomura Y, Ishii Y, Tano Y.
    Invest Ophthalmol Vis Sci; 1998 Sep 01; 39(10):1947-53. PubMed ID: 9727418
    [Abstract] [Full Text] [Related]

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