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Journal Abstract Search

141 related items for PubMed ID: 8872482

  • 1. A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.
    del Castillo I, Villamar M, Sarduy M, Romero L, Herraiz C, Hernández FJ, Rodríguez M, Borrás I, Montero A, Bellón J, Tapia MC, Moreno F.
    Hum Mol Genet; 1996 Sep; 5(9):1383-7. PubMed ID: 8872482
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  • 2. Refinement of the locus for non-syndromic sensorineural deafness (DFN2).
    Cui B, Zhang H, Lu Y, Zhong W, Pei G, Kong X, Hu L.
    J Genet; 2004 Apr; 83(1):35-8. PubMed ID: 15240907
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  • 3. Mapping of DFN2 to Xq22.
    Tyson J, Bellman S, Newton V, Simpson P, Malcolm S, Pembrey ME, Bitner-Glindzicz M.
    Hum Mol Genet; 1996 Dec; 5(12):2055-60. PubMed ID: 8968763
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  • 4. A new nonsyndromic X-linked sensorineural hearing impairment linked to Xp21.2.
    Lalwani AK, Brister JR, Fex J, Grundfast KM, Pikus AT, Ploplis B, San Agustin T, Skarka H, Wilcox ER.
    Am J Hum Genet; 1994 Oct; 55(4):685-94. PubMed ID: 7942846
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  • 6. A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22.
    Tranebjaerg L, Schwartz C, Eriksen H, Andreasson S, Ponjavic V, Dahl A, Stevenson RE, May M, Arena F, Barker D.
    J Med Genet; 1995 Apr; 32(4):257-63. PubMed ID: 7643352
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  • 9. [Gene mapping for autosomal dominant nonsyndromic hearing loss DFNA11].
    Yuan H, Han DY, Wang QJ, Zong L, Zhao YL.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Jun; 42(6):422-7. PubMed ID: 17702415
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  • 11. A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.
    Ansar M, Din MA, Arshad M, Sohail M, Faiyaz-Ul-Haque M, Haque S, Ahmad W, Leal SM.
    Eur J Hum Genet; 2003 Jan; 11(1):77-80. PubMed ID: 12529709
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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; 20(5):621-6. PubMed ID: 10503584
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  • 15. Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.
    Farah WI, Aminuddin BS, Ruszymah BH.
    Malays J Pathol; 2006 Jun; 28(1):23-33. PubMed ID: 17694956
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  • 16. Clinical and genetic heterogeneity in X-linked deafness.
    Reardon W, Middleton-Price HR, Malcolm S, Phelps P, Bellman S, Luxon L, Martin JA, Bumby A, Pembrey ME.
    Br J Audiol; 1992 Apr; 26(2):109-14. PubMed ID: 1628115
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  • 20. Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness.
    Mustapha M, Salem N, Weil D, el-Zir E, Loiselet J, Petit C.
    Eur J Hum Genet; 1998 Apr; 6(6):548-51. PubMed ID: 9887371
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