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Journal Abstract Search

194 related items for PubMed ID: 7616540

  • 21. Assignment of the gene for complete X-linked congenital stationary night blindness (CSNB1) to Xp11.3.
    Musarella MA, Weleber RG, Murphey WH, Young RS, Anson-Cartwright L, Mets M, Kraft SP, Polemeno R, Litt M, Worton RG.
    Genomics; 1989 Nov; 5(4):727-37. PubMed ID: 2574143
    [Abstract] [Full Text] [Related]

  • 22. Phenotypic characterization of complete CSNB in the inbred research beagle: how common is CSNB in research and companion dogs?
    Oh A, Loew ER, Foster ML, Davidson MG, English RV, Gervais KJ, Herring IP, Mowat FM.
    Doc Ophthalmol; 2018 Oct; 137(2):87-101. PubMed ID: 30051304
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  • 23. Clinical and electroretinographic comparison between Aland Island eye disease and a newly found related disease with X-chromosomal inheritance.
    Carlson S, Vesti E, Raitta C, Donner M, Eriksson AW, Forsius H.
    Acta Ophthalmol (Copenh); 1991 Dec; 69(6):703-10. PubMed ID: 1789083
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  • 24. Congenital stationary night blindness with hypoplastic discs, negative electroretinogram and thinning of the inner nuclear layer.
    Al Oreany AA, Al Hadlaq A, Schatz P.
    Graefes Arch Clin Exp Ophthalmol; 2016 Oct; 254(10):1951-1956. PubMed ID: 27084085
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  • 26. [Electrophysiologic tests for diagnosis of congenital night blindness].
    Lubiński W, Palacz A, Penkala K, Palacz O.
    Klin Oczna; 1996 Jan; 98(1):9-12. PubMed ID: 9019583
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  • 28. Affected females in X-linked congenital stationary night blindness.
    Ruttum MS, Lewandowski MF, Bateman JB.
    Ophthalmology; 1992 May; 99(5):747-52. PubMed ID: 1594221
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  • 29. Variable expressivity in X-linked congenital stationary night blindness.
    Pearce WG, Reedyk M, Coupland SG.
    Can J Ophthalmol; 1990 Feb; 25(1):3-10. PubMed ID: 2328435
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  • 30. Electroretinogram in Duchenne/Becker muscular dystrophy.
    Pascual Pascual SI, Molano J, Pascual-Castroviejo I.
    Pediatr Neurol; 1998 Apr; 18(4):315-20. PubMed ID: 9588526
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  • 32. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep; 30(9):737-44. PubMed ID: 8411068
    [Abstract] [Full Text] [Related]

  • 33. Novel CACNA1F mutations in Japanese patients with incomplete congenital stationary night blindness.
    Nakamura M, Ito S, Terasaki H, Miyake Y.
    Invest Ophthalmol Vis Sci; 2001 Jun; 42(7):1610-6. PubMed ID: 11381068
    [Abstract] [Full Text] [Related]

  • 34. ERG characteristics of congenital stationary night blindness.
    Wu D, Xu X, Wu L, Luo T.
    Yan Ke Xue Bao; 1990 Jun; 6(1-2):32-5. PubMed ID: 2101357
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  • 38. Congenital stationary night blindness with negative electroretinogram. A new classification.
    Miyake Y, Yagasaki K, Horiguchi M, Kawase Y, Kanda T.
    Arch Ophthalmol; 1986 Jul; 104(7):1013-20. PubMed ID: 3488053
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  • 39. Autosomal dominant congenital stationary night blindness and normal fundus with an electronegative electroretinogram.
    Noble KG, Carr RE, Siegel IM.
    Am J Ophthalmol; 1990 Jan 15; 109(1):44-8. PubMed ID: 2297031
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