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Journal Abstract Search

235 related items for PubMed ID: 1301915

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  • 3. 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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  • 5. Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneity.
    Farrar GJ, McWilliam P, Bradley DG, Kenna P, Lawler M, Sharp EM, Humphries MM, Eiberg H, Conneally PM, Trofatter JA.
    Genomics; 1990 Sep; 8(1):35-40. PubMed ID: 2081598
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  • 7. 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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  • 8. 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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  • 10. 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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  • 11. Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish origin.
    Jordan SA, Farrar GJ, Kumar-Singh R, Kenna P, Humphries MM, Allamand V, Sharp EM, Humphries P.
    Am J Hum Genet; 1992 Mar; 50(3):634-9. PubMed ID: 1539599
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  • 13. 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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  • 16. A 3-bp deletion in the rhodopsin gene in a family with autosomal dominant retinitis pigmentosa.
    Inglehearn CF, Bashir R, Lester DH, Jay M, Bird AC, Bhattacharya SS.
    Am J Hum Genet; 1991 Jan; 48(1):26-30. PubMed ID: 1985460
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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 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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