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Journal Abstract Search

159 related items for PubMed ID: 7847373

  • 21. A novel mutation in the ABCR gene in four patients with autosomal recessive Stargardt disease.
    Zhang K, Garibaldi DC, Kniazeva M, Albini T, Chiang MF, Kerrigan M, Sunness JS, Han M, Allikmets R.
    Am J Ophthalmol; 1999 Dec; 128(6):720-4. PubMed ID: 10612508
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  • 23. Fundus flavimaculatus: polymorphic retinal change in siblings.
    Isashiki Y, Ohba N.
    Br J Ophthalmol; 1985 Jul; 69(7):522-4. PubMed ID: 4016047
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  • 24. Autosomal dominant macular atrophy at 6q14 excludes CORD7 and MCDR1/PBCRA loci.
    Griesinger IB, Sieving PA, Ayyagari R.
    Invest Ophthalmol Vis Sci; 2000 Jan; 41(1):248-55. PubMed ID: 10634627
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  • 25. A 5-bp deletion in ELOVL4 is associated with two related forms of autosomal dominant macular dystrophy.
    Zhang K, Kniazeva M, Han M, Li W, Yu Z, Yang Z, Li Y, Metzker ML, Allikmets R, Zack DJ, Kakuk LE, Lagali PS, Wong PW, MacDonald IM, Sieving PA, Figueroa DJ, Austin CP, Gould RJ, Ayyagari R, Petrukhin K.
    Nat Genet; 2001 Jan; 27(1):89-93. PubMed ID: 11138005
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  • 28. Genetic fine mapping of the gene for recessive Stargardt disease.
    Hoyng CB, Poppelaars F, van de Pol TJ, Kremer H, Pinckers AJ, Deutman AF, Cremers FP.
    Hum Genet; 1996 Oct; 98(4):500-4. PubMed ID: 8792830
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  • 31. Stargardt's disease is not allelic to the genes for neuronal ceroid lipofuscinoses.
    Gerber S, Odent S, Postel-Vinay A, Janin N, Dufier JL, Munnich A, Frezal J, Kaplan J.
    J Med Genet; 1994 Mar; 31(3):222-3. PubMed ID: 8014971
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  • 33. Long-term follow-up of dominant macular dystrophy with flecks (Stargardt).
    Mansour AM.
    Ophthalmologica; 1992 Mar; 205(3):138-43. PubMed ID: 1475092
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  • 36. Assessment of the interphotoreceptor matrix proteoglycan-1 (IMPG1) gene localised to 6q13-q15 in autosomal dominant Stargardt-like disease (ADSTGD), progressive bifocal chorioretinal atrophy (PBCRA), and North Carolina macular dystrophy (MCDR1).
    Gehrig A, Felbor U, Kelsell RE, Hunt DM, Maumenee IH, Weber BH.
    J Med Genet; 1998 Aug; 35(8):641-5. PubMed ID: 9719369
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  • 38. The gene responsible for autosomal dominant Doyne's honeycomb retinal dystrophy (DHRD) maps to chromosome 2p16.
    Gregory CY, Evans K, Wijesuriya SD, Kermani S, Jay MR, Plant C, Cox N, Bird AC, Bhattacharya SS.
    Hum Mol Genet; 1996 Jul; 5(7):1055-9. PubMed ID: 8817347
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