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Journal Abstract Search

203 related items for PubMed ID: 2328435

  • 1. 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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  • 2. 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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  • 3. 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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  • 4. Aland eye disease (Forsius-Eriksson-Miyake syndrome) with probability established in a Danish family.
    Rosenberg T, Schwartz M, Simonsen SE.
    Acta Ophthalmol (Copenh); 1990 Jun; 68(3):281-91. PubMed ID: 2392903
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  • 7. Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23.
    Bech-Hansen NT, Boycott KM, Gratton KJ, Ross DA, Field LL, Pearce WG.
    Hum Genet; 1998 Aug; 103(2):124-30. PubMed ID: 9760193
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  • 8. [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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  • 10. 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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  • 12. 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 15; 52(1):71-7. PubMed ID: 8434607
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  • 16. A phenotypic study of congenital stationary night blindness (CSNB) associated with mutations in the GRM6 gene.
    Sergouniotis PI, Robson AG, Li Z, Devery S, Holder GE, Moore AT, Webster AR.
    Acta Ophthalmol; 2012 May 15; 90(3):e192-7. PubMed ID: 22008250
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  • 17. Clinical findings in patients with congenital stationary night blindness of the Schubert-Bornschein type.
    Ruether K, Apfelstedt-Sylla E, Zrenner E.
    Ger J Ophthalmol; 1993 Nov 15; 2(6):429-35. PubMed ID: 8312830
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  • 18. Paradoxical pupillary responses in congenital stationary night blindness.
    Barricks ME, Flynn JT, Kushner BJ.
    Arch Ophthalmol; 1977 Oct 15; 95(10):1800-4. PubMed ID: 303092
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