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Pubmed for Handhelds

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Journal Abstract Search

182 related items for PubMed ID: 11073537

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  • 2. 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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  • 3. 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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  • 4. 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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  • 8. 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; 12(4):421-3. PubMed ID: 8630497
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  • 9. 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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  • 10. 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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  • 11. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 17. [Genetic aspects of deafness].
    Dallapiccola B, Mingarelli R, Gennarelli M, Novelli G.
    Acta Otorhinolaryngol Ital; 1996 Apr; 16(2):79-90. PubMed ID: 8766069
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