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Journal Abstract Search

178 related items for PubMed ID: 9760193

  • 1.
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  • 2. Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
    Boycott KM, Pearce WG, Musarella MA, Weleber RG, Maybaum TA, Birch DG, Miyake Y, Young RS, Bech-Hansen NT.
    Am J Hum Genet; 1998 Apr; 62(4):865-75. PubMed ID: 9529339
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  • 7. Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.
    Bech-Hansen NT, Pearce WG.
    Am J Hum Genet; 1993 Jan; 52(1):71-7. PubMed ID: 8434607
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  • 8. Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.
    Boycott KM, Pearce WG, Bech-Hansen NT.
    Can J Ophthalmol; 2000 Jun; 35(4):204-13. PubMed ID: 10900517
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  • 9. Complete congenital stationary night blindness maps on Xp11.4 in a Sardinian family.
    Rozzo C, Fossarello M, Galleri G, Miano MG, Ciccodicola A, Sole G, Pirastu M.
    Eur J Hum Genet; 1999 Jul; 7(5):574-8. PubMed ID: 10439964
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  • 10. Genotype and phenotype of 101 dutch patients with congenital stationary night blindness.
    Bijveld MM, Florijn RJ, Bergen AA, van den Born LI, Kamermans M, Prick L, Riemslag FC, van Schooneveld MJ, Kappers AM, van Genderen MM.
    Ophthalmology; 2013 Oct; 120(10):2072-81. PubMed ID: 23714322
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  • 11. 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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  • 14. [Incomplete congenital stationary night blindness (CSNB). An important differential diagnosis of congenital nystagmus].
    Lorenz B, Andrassi M, Miliczek KD.
    Klin Monbl Augenheilkd; 1996 Jan; 208(1):48-55. PubMed ID: 8839345
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  • 15. Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.
    Bech-Hansen NT, Moore BJ, Pearce WG.
    Genomics; 1992 Feb; 12(2):409-11. PubMed ID: 1740347
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  • 16. Abnormalities of the long flash ERG in congenital stationary night blindness of the Schubert-Bornschein type.
    Langrová H, Gamer D, Friedburg C, Besch D, Zrenner E, Apfelstedt-Sylla E.
    Vision Res; 2002 May; 42(11):1475-83. PubMed ID: 12044753
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  • 18. Duchenne muscular dystrophy: negative electroretinograms and normal dark adaptation. Reappraisal of assignment of X linked incomplete congenital stationary night blindness.
    Jensen H, Warburg M, Sjö O, Schwartz M.
    J Med Genet; 1995 May; 32(5):348-51. PubMed ID: 7616540
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  • 19. [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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  • 20. Riggs-type dominant congenital stationary night blindness: ERG findings, a new GNAT1 mutation and a systemic association.
    Marmor MF, Zeitz C.
    Doc Ophthalmol; 2018 Aug; 137(1):57-62. PubMed ID: 30051303
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