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Journal Abstract Search

144 related items for PubMed ID: 6364465

  • 1.
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  • 2. X-linked recessive congenital stationary night blindness, myopia, and tilted discs.
    Hittner HM, Borda RP, Justice J.
    J Pediatr Ophthalmol Strabismus; 1981; 18(1):15-20. PubMed ID: 6972443
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  • 3. X-linked congenital stationary night blindness. Review and report of a family with hyperopia.
    Khouri G, Mets MB, Smith VC, Wendell M, Pass AS.
    Arch Ophthalmol; 1988 Oct; 106(10):1417-22. PubMed ID: 3052384
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  • 4. The photopic electroretinogram in congenital stationary night blindness with myopia.
    Lachapelle P, Little JM, Polomeno RC.
    Invest Ophthalmol Vis Sci; 1983 Apr; 24(4):442-50. PubMed ID: 6601088
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  • 8. 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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  • 11. 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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  • 12. Linkage analysis in a family with complete type congenital stationary night blindness with and without myopia.
    Dry KL, Van Dorp DB, Aldred MA, Brown J, Hardwick LJ, Wright AF.
    Clin Genet; 1993 May; 43(5):250-4. PubMed ID: 8375106
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  • 14. Aland island eye disease: clinical and electrophysiological studies of a Welsh family.
    Hawksworth NR, Headland S, Good P, Thomas NS, Clarke A.
    Br J Ophthalmol; 1995 May; 79(5):424-30. PubMed ID: 7612552
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  • 16. [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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  • 19. [Congenital stationary night blindness (CSNB)--a case report].
    Liláková D, Svĕrák J, Hejcmanová D.
    Cesk Slov Oftalmol; 2005 May; 61(3):218-23. PubMed ID: 15981496
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  • 20. An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness.
    Strom TM, Nyakatura G, Apfelstedt-Sylla E, Hellebrand H, Lorenz B, Weber BH, Wutz K, Gutwillinger N, Rüther K, Drescher B, Sauer C, Zrenner E, Meitinger T, Rosenthal A, Meindl A.
    Nat Genet; 1998 Jul; 19(3):260-3. PubMed ID: 9662399
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