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Journal Abstract Search

98 related items for PubMed ID: 8364569

  • 1. Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8).
    Kumar-Singh R, Farrar GJ, Mansergh F, Kenna P, Bhattacharya S, Gal A, Humphries P.
    Hum Mol Genet; 1993 Jul; 2(7):875-8. PubMed ID: 8364569
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  • 2. Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locus.
    Jordan SA, del Rio T, Soriano N, Garcia-Sandoval B, Kenna P, Ayuso C, Benitez J, Humphries P.
    Hum Mol Genet; 1992 Sep; 1(6):411-5. PubMed ID: 1301915
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  • 3. Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: further locus heterogeneity in adRP.
    Bashir R, Inglehearn CF, Keen TJ, Lindsey J, Atif U, Carter SA, Stephenson AM, Jackson A, Jay M, Bird AC.
    Genomics; 1992 Sep; 14(1):191-3. PubMed ID: 1427827
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  • 4. Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3.
    McWilliam P, Farrar GJ, Kenna P, Bradley DG, Humphries MM, Sharp EM, McConnell DJ, Lawler M, Sheils D, Ryan C.
    Genomics; 1989 Oct; 5(3):619-22. PubMed ID: 2613244
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  • 5. An eighth locus for autosomal dominant retinitis pigmentosa is linked to chromosome 17q.
    Bardien S, Ebenezer N, Greenberg J, Inglehearn CF, Bartmann L, Goliath R, Beighton P, Ramesar R, Bhattacharya SS.
    Hum Mol Genet; 1995 Aug; 4(8):1459-62. PubMed ID: 7581389
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  • 7. Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6.
    Farrar GJ, Jordan SA, Kenna P, Humphries MM, Kumar-Singh R, McWilliam P, Allamand V, Sharp E, Humphries P.
    Genomics; 1991 Dec; 11(4):870-4. PubMed ID: 1783395
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  • 8. Recombination between rhodopsin and locus D3S47 (C17) in rhodopsin retinitis pigmentosa families.
    Inglehearn CF, Lester DH, Bashir R, Atif U, Keen TJ, Sertedaki A, Lindsey J, Jay M, Bird AC, Farrar GJ.
    Am J Hum Genet; 1992 Mar; 50(3):590-7. PubMed ID: 1539595
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  • 9. A linkage survey of 20 dominant retinitis pigmentosa families: frequencies of the nine known loci and evidence for further heterogeneity.
    Inglehearn CF, Tarttelin EE, Plant C, Peacock RE, al-Maghtheh M, Vithana E, Bird AC, Bhattacharya SS.
    J Med Genet; 1998 Jan; 35(1):1-5. PubMed ID: 9475085
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  • 10. Map refinement of locus RP13 to human chromosome 17p13.3 in a second family with autosomal dominant retinitis pigmentosa.
    Kojis TL, Heinzmann C, Flodman P, Ngo JT, Sparkes RS, Spence MA, Bateman JB, Heckenlively JR.
    Am J Hum Genet; 1996 Feb; 58(2):347-55. PubMed ID: 8571961
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  • 12. Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosa.
    Kumar-Singh R, Kenna PF, Farrar GJ, Humphries P.
    Genomics; 1993 Jan; 15(1):212-5. PubMed ID: 8432539
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  • 13. A new locus for autosomal dominant retinitis pigmentosa on the short arm of chromosome 17.
    Greenberg J, Goliath R, Beighton P, Ramesar R.
    Hum Mol Genet; 1994 Jun; 3(6):915-8. PubMed ID: 7951236
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  • 16. Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21.
    Farrar GJ, McWilliam P, Sharp EM, Kenna P, Bradley DG, Humphries MM, McConnell DJ, Humphries P.
    Genomics; 1989 Oct; 5(3):612-8. PubMed ID: 2613243
    [Abstract] [Full Text] [Related]

  • 17. Linkage mapping of autosomal dominant retinitis pigmentosa (RP1) to the pericentric region of human chromosome 8.
    Blanton SH, Heckenlively JR, Cottingham AW, Friedman J, Sadler LA, Wagner M, Friedman LH, Daiger SP.
    Genomics; 1991 Dec; 11(4):857-69. PubMed ID: 1783394
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  • 18. Retinitis pigmentosa: genetic mapping in X-linked and autosomal forms of the disease.
    Humphries P, Farrar GJ, Kenna P, McWilliam P.
    Clin Genet; 1990 Jul; 38(1):1-13. PubMed ID: 2201466
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  • 19. A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1.
    Xu SY, Schwartz M, Rosenberg T, Gal A.
    Hum Mol Genet; 1996 Aug; 5(8):1193-7. PubMed ID: 8842740
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  • 20. Autosomal dominant retinitis pigmentosa: no evidence for nonallelic genetic heterogeneity on 3q.
    Kumar-Singh R, Wang H, Humphries P, Farrar GJ.
    Am J Hum Genet; 1993 Feb; 52(2):319-26. PubMed ID: 8430695
    [Abstract] [Full Text] [Related]

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