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Journal Abstract Search

120 related items for PubMed ID: 9126484

  • 1. Linkage analysis of progressive hearing loss in five extended families maps the DFNA2 gene to a 1.25-Mb region on chromosome 1p.
    Van Camp G, Coucke PJ, Kunst H, Schatteman I, Van Velzen D, Marres H, van Ewijk M, Declau F, Van Hauwe P, Meyers J, Kenyon J, Smith SD, Smith RJ, Djelantik B, Cremers CW, Van de Heyning PH, Willems PJ.
    Genomics; 1997 Apr 01; 41(1):70-4. PubMed ID: 9126484
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  • 3. Further evidence for a third deafness gene within the DFNA2 locus.
    Goldstein JA, Lalwani AK.
    Am J Med Genet; 2002 Apr 01; 108(4):304-9. PubMed ID: 11920835
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  • 7. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
    Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C.
    Eur J Hum Genet; 2002 Mar 01; 10(3):210-2. PubMed ID: 11973626
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  • 9. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
    Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K.
    J Hum Genet; 2002 Mar 01; 47(12):635-40. PubMed ID: 12522684
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  • 11. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.
    Coyle B, Coffey R, Armour JA, Gausden E, Hochberg Z, Grossman A, Britton K, Pembrey M, Reardon W, Trembath R.
    Nat Genet; 1996 Apr 01; 12(4):421-3. PubMed ID: 8630497
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  • 13. The gene for Pendred syndrome is located between D7S501 and D7S692 in a 1.7-cM region on chromosome 7q.
    Coucke P, Van Camp G, Demirhan O, Kabakkaya Y, Balemans W, Van Hauwe P, Van Agtmael T, Smith RJ, Parving A, Bolder CH, Cremers CW, Willems PJ.
    Genomics; 1997 Feb 15; 40(1):48-54. PubMed ID: 9070918
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  • 14. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
    Manolis EN, Eavey RD, Sangwatanaroj S, Halpin C, Rosenbaum S, Watkins H, Jarcho J, Seidman CE, Seidman JG.
    Am J Otol; 1999 Sep 15; 20(5):621-6. PubMed ID: 10503584
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  • 15. The telomere of human chromosome 1p contains at least two independent autosomal dominant congenital cataract genes.
    McKay JD, Patterson B, Craig JE, Russell-Eggitt IM, Wirth MG, Burdon KP, Hewitt AW, Cohn AC, Kerdraon Y, Mackey DA.
    Br J Ophthalmol; 2005 Jul 15; 89(7):831-4. PubMed ID: 15965161
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  • 16. First genomic localization of oculo-oto-dental syndrome with linkage to chromosome 20q13.1.
    Vieira H, Gregory-Evans K, Lim N, Brookes JL, Brueton LA, Gregory-Evans CY.
    Invest Ophthalmol Vis Sci; 2002 Aug 15; 43(8):2540-5. PubMed ID: 12147582
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  • 18. Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to chromosome region 7q31.
    Greinwald JH, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S, Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ.
    Am J Med Genet; 1998 Jun 30; 78(2):107-13. PubMed ID: 9674898
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