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Journal Abstract Search

83 related items for PubMed ID: 8792830

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  • 2. A YAC contig encompassing the recessive Stargardt disease gene (STGD) on chromosome 1p.
    Anderson KL, Baird L, Lewis RA, Chinault AC, Otterud B, Leppert M, Lupski JR.
    Am J Hum Genet; 1995 Dec; 57(6):1351-63. PubMed ID: 8533764
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  • 11. The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration.
    Zhang K, Kniazeva M, Hutchinson A, Han M, Dean M, Allikmets R.
    Genomics; 1999 Sep 01; 60(2):234-7. PubMed ID: 10486215
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  • 13. Structure and physical mapping of DR1, a TATA-binding protein-associated phosphoprotein gene, to chromosome 1p22.1 and its exclusion in Stargardt disease (STGD).
    Rozet JM, Gerber S, Perrault I, Camuzat A, Calvas P, Viegas-Pequignot E, Molina-Gomes D, Le Paslier D, Chumakov I, Munnich A, Kaplan J.
    Genomics; 1996 Sep 15; 36(3):554-6. PubMed ID: 8884286
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  • 14. The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.
    Diaz GA, Khan KT, Gelb BD.
    Genomics; 1998 Nov 15; 54(1):13-8. PubMed ID: 9806825
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  • 15. Exclusion of the cone-specific alpha-subunit of the transducin gene in Stargardt's disease.
    Gerber S, Rozet JM, Bonneau D, Souied E, Weissenbach J, Frezal J, Munnich A, Kaplan J.
    Hum Genet; 1995 Apr 15; 95(4):382-4. PubMed ID: 7705831
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  • 18. Clinical features of a Stargardt-like dominant progressive macular dystrophy with genetic linkage to chromosome 6q.
    Stone EM, Nichols BE, Kimura AE, Weingeist TA, Drack A, Sheffield VC.
    Arch Ophthalmol; 1994 Jun 15; 112(6):765-72. PubMed ID: 8002834
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  • 19. Localization of the gene for dominant cystoid macular dystrophy on chromosome 7p.
    Kremer H, Pinckers A, van den Helm B, Deutman AF, Ropers HH, Mariman EC.
    Hum Mol Genet; 1994 Feb 15; 3(2):299-302. PubMed ID: 8004098
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  • 20. Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.
    Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA.
    Am J Hum Genet; 2000 Jul 15; 67(1):222-8. PubMed ID: 10820129
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