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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 [Abstract] [Full Text] [Related]
13. 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 [Abstract] [Full Text] [Related]
15. [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 [Abstract] [Full Text] [Related]
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