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Journal Abstract Search

208 related items for PubMed ID: 7902160

  • 1. Allelic association and linkage studies in Wilson disease.
    Thomas GR, Roberts EA, Rosales TO, Moroz SP, Lambert MA, Wong LT, Cox DW.
    Hum Mol Genet; 1993 Sep; 2(9):1401-5. PubMed ID: 7902160
    [Abstract] [Full Text] [Related]

  • 2. A 4.5-megabase yeast artificial chromosome contig from human chromosome 13q14.3 ordering 9 polymorphic microsatellites (22 sequence-tagged sites) tightly linked to the Wilson disease locus.
    White A, Tomfohrde J, Stewart E, Barnes R, Le Paslier D, Weissenbach J, Cavalli-Sforza L, Farrer L, Bowcock A.
    Proc Natl Acad Sci U S A; 1993 Nov 01; 90(21):10105-9. PubMed ID: 8234264
    [Abstract] [Full Text] [Related]

  • 3. Long range restriction mapping of 13q14.3 focused on the Wilson disease region.
    Bull PC, Cox DW.
    Genomics; 1993 Jun 01; 16(3):593-8. PubMed ID: 8325631
    [Abstract] [Full Text] [Related]

  • 4. Polymorphic microsatellites and Wilson disease (WD).
    Stewart EA, White A, Tomfohrde J, Osborne-Lawrence S, Prestridge L, Bonne-Tamir B, Scheinberg IH, St George-Hyslop P, Giagheddu M, Kim JW.
    Am J Hum Genet; 1993 Oct 01; 53(4):864-73. PubMed ID: 8213814
    [Abstract] [Full Text] [Related]

  • 5. Identification of crossovers in Wilson disease families as reference points for a genetic localization of the gene.
    Scheffer H, Houwen RH, Te Meerman GJ, Loessner J, Bachmann B, Kunert E, Verlind E, Buys CH.
    Hum Genet; 1992 Aug 01; 89(6):607-11. PubMed ID: 1511977
    [Abstract] [Full Text] [Related]

  • 6. Refining the position of Wilson disease by linkage disequilibrium with polymorphic microsatellites.
    Bowcock AM, Tomfohrde J, Weissenbach J, Bonne-Tamir B, St George-Hyslop P, Giagheddu M, Cavalli-Sforza LL, Farrer LA.
    Am J Hum Genet; 1994 Jan 01; 54(1):79-87. PubMed ID: 8279473
    [Abstract] [Full Text] [Related]

  • 7. Haplotype studies in Wilson disease.
    Thomas GR, Bull PC, Roberts EA, Walshe JM, Cox DW.
    Am J Hum Genet; 1994 Jan 01; 54(1):71-8. PubMed ID: 8279472
    [Abstract] [Full Text] [Related]

  • 8. Mapping the Wilson disease locus to a cluster of linked polymorphic markers on chromosome 13.
    Bowcock AM, Farrer LA, Cavalli-Sforza LL, Hebert JM, Kidd KK, Frydman M, Bonne-Tamir B.
    Am J Hum Genet; 1987 Jul 01; 41(1):27-35. PubMed ID: 3474893
    [Abstract] [Full Text] [Related]

  • 9. Eight closely linked loci place the Wilson disease locus within 13q14-q21.
    Bowcock AM, Farrer LA, Hebert JM, Agger M, Sternlieb I, Scheinberg IH, Buys CH, Scheffer H, Frydman M, Chajek-Saul T.
    Am J Hum Genet; 1988 Nov 01; 43(5):664-74. PubMed ID: 3189332
    [Abstract] [Full Text] [Related]

  • 10. Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.
    Haines JL, Ozelius L, St George-Hyslop P, Wexler NS, Gusella JF, Conneally PM.
    Genet Epidemiol; 1988 Nov 01; 5(6):375-80. PubMed ID: 2905314
    [Abstract] [Full Text] [Related]

  • 11. Predictive testing for Wilson's disease using tightly linked and flanking DNA markers.
    Farrer LA, Bowcock AM, Hebert JM, Bonné-Tamir B, Sternlieb I, Giagheddu M, St George-Hyslop P, Frydman M, Lössner J, Demelia L.
    Neurology; 1991 Jul 01; 41(7):992-9. PubMed ID: 2067662
    [Abstract] [Full Text] [Related]

  • 12. Close linkage of the Wilson's disease locus to D13S12 in the chromosomal region 13q21 and not to ESD in 13q14.
    Houwen RH, Scheffer H, te Meerman GJ, van der Vlies P, Buys CH.
    Hum Genet; 1990 Oct 01; 85(5):560-2. PubMed ID: 2227943
    [Abstract] [Full Text] [Related]

  • 13. Isolation of new probes in the region of the Wilson disease locus, 13q14.2-->q14.3.
    Bull PC, Barwell JA, Hannah HT, Pautler SE, Higgins MJ, Lalande M, Cox DW.
    Cytogenet Cell Genet; 1993 Oct 01; 64(1):12-7. PubMed ID: 8508673
    [Abstract] [Full Text] [Related]

  • 14. Carrier detection and early diagnosis of Wilson's disease by restriction fragment length polymorphism analysis.
    Figus A, Lampis R, Devoto M, Ristaldi MS, Ideo A, de Virgilis S, Nurchi AM, Corrias A, Corda R, Lai ME.
    J Med Genet; 1989 Feb 01; 26(2):78-82. PubMed ID: 2563776
    [Abstract] [Full Text] [Related]

  • 15. Mapping, cloning and genetic characterization of the region containing the Wilson disease gene.
    Petrukhin K, Fischer SG, Pirastu M, Tanzi RE, Chernov I, Devoto M, Brzustowicz LM, Cayanis E, Vitale E, Russo JJ.
    Nat Genet; 1993 Dec 01; 5(4):338-43. PubMed ID: 8298640
    [Abstract] [Full Text] [Related]

  • 16. Physical localisation of the chromosomal marker D13S31 places the Wilson disease locus at the junction of bands q14.3 and q21.1 of chromosome 13.
    Kooy RF, Van der Veen AY, Verlind E, Houwen RH, Scheffer H, Buys CH.
    Hum Genet; 1993 Jun 01; 91(5):504-6. PubMed ID: 8314565
    [Abstract] [Full Text] [Related]

  • 17. A deletion hybrid breakpoint map of the chromosomal region 13q14-q21 orders 19 genetic markers in 10 intervals.
    Kooy RF, Verlind E, Houwen RH, Shapiro DN, Hawthorn LA, Cowell JK, Scheffer H, Buys CH.
    Eur J Hum Genet; 1994 Jun 01; 2(1):59-65. PubMed ID: 7913868
    [Abstract] [Full Text] [Related]

  • 18. DNA markers for the diagnosis of Wilson disease.
    Houwen RH, Roberts EA, Thomas GR, Cox DW.
    J Hepatol; 1993 Mar 01; 17(3):269-76. PubMed ID: 8100247
    [Abstract] [Full Text] [Related]

  • 19. Predicting genotypes at loci for autosomal recessive disorders using linked genetic markers: application to Wilson's disease.
    Farrer LA, Bonne-Tamir B, Frydman M, Magazanik A, Kidd KK, Bowcock AM, Cavalli-Sforza LL.
    Hum Genet; 1988 Jun 01; 79(2):109-17. PubMed ID: 3164701
    [Abstract] [Full Text] [Related]

  • 20. Esterase D and retinoblastoma gene loci are tightly linked to Wilson's disease in Chinese pedigrees from Taiwan.
    Chuang LM, Tai TY, Wang TR, Chang YC, Chen KH, Lin RS, Lin BJ.
    Hum Genet; 1991 Aug 01; 87(4):465-8. PubMed ID: 1679032
    [Abstract] [Full Text] [Related]

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