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Journal Abstract Search

114 related items for PubMed ID: 7891371

  • 1.
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  • 2. Deletion mapping of the DXS986, DXS995, and DXS1002 loci defines their order within Xq21.
    Clark PA, Lester T, Villard L, Fontes M, Kinnon C.
    J Med Genet; 1994 Apr; 31(4):344-5. PubMed ID: 8071966
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  • 3. X-linked mixed deafness with stapes fixation in a Mauritian kindred: linkage to Xq probe pDP34.
    Wallis C, Ballo R, Wallis G, Beighton P, Goldblatt J.
    Genomics; 1988 Nov; 3(4):299-301. PubMed ID: 3243543
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  • 4. The gene for X-linked progressive mixed deafness with perilymphatic gusher during stapes surgery (DFN3) is linked to PGK.
    Brunner HG, van Bennekom A, Lambermon EM, Oei TL, Cremers WR, Wieringa B, Ropers HH.
    Hum Genet; 1988 Dec; 80(4):337-40. PubMed ID: 2904400
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  • 5. Genetic linkage analysis of familial amyotrophic lateral sclerosis using human chromosome 21 microsatellite DNA markers.
    Rosen DR, Sapp P, O'Regan J, McKenna-Yasek D, Schlumpf KS, Haines JL, Gusella JF, Horvitz HR, Brown RH.
    Am J Med Genet; 1994 May 15; 51(1):61-9. PubMed ID: 7913294
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  • 6. Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.
    Reardon W, Roberts S, Phelps PD, Thomas NS, Beck L, Issac R, Hughes HE.
    Am J Med Genet; 1992 Nov 01; 44(4):513-7. PubMed ID: 1442898
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  • 7. Linkage analyses between dominant X-linked Charcot-Marie-Tooth disease, and 15 Xq11-Xq21 microsatellites in a new large family: three new markers are closely linked to the gene.
    Le Guern E, Ravise N, Gugenheim M, Vignal A, Penet C, Bouche P, Weissenbach J, Agid Y, Brice A.
    Neuromuscul Disord; 1994 Nov 01; 4(5-6):463-9. PubMed ID: 7881290
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  • 11. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene.
    Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M, Petit C.
    Hum Mol Genet; 1994 Jun 01; 3(6):989-93. PubMed ID: 7951250
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  • 12. X linked myotubular myopathy (MTM1) maps between DXS304 and DXS305, closely linked to the DXS455 VNTR and a new, highly informative microsatellite marker (DXS1684).
    Dahl N, Samson F, Thomas NS, Hu LJ, Gong W, Herman G, Laporte J, Kioschis P, Poustka A, Mandel JL.
    J Med Genet; 1994 Dec 01; 31(12):922-4. PubMed ID: 7891372
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  • 13. A family with X-linked deafness showing linkage to the proximal Xq region of the X chromosome.
    Robinson D, Lamont M, Curtis G, Shields DC, Phelps P.
    Hum Genet; 1992 Nov 01; 90(3):316-8. PubMed ID: 1362559
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  • 15. Fragile X syndrome: diagnosis using highly polymorphic microsatellite markers.
    Richards RI, Shen Y, Holman K, Kozman H, Hyland VJ, Mulley JC, Sutherland GR.
    Am J Hum Genet; 1991 Jun 01; 48(6):1051-7. PubMed ID: 2035525
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  • 18. Novel RFLPs and microsatellite repeats increase informativity at four loci mapping to Xq22-q25.
    Newton R, Stanier P, Forbes S, Moore GE.
    Hum Genet; 1994 Feb 01; 93(2):218-21. PubMed ID: 7906669
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  • 19. Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22.
    Thiselton DL, Lindsay S, Kamakari S, Hardcastle AJ, Roustan P, Bhattacharya SS.
    Genomics; 1995 Jan 01; 25(1):279-81. PubMed ID: 7774929
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  • 20. Fine mapping of the human SCIDX1 locus at Xq12-13.1.
    Markiewicz S, DiSanto JP, Chelly J, Fairweather N, Le Marec B, Griscelli C, Graeber MB, Müller U, Fischer A, Monaco AP.
    Hum Mol Genet; 1993 Jun 01; 2(6):651-4. PubMed ID: 8353486
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