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Journal Abstract Search

185 related items for PubMed ID: 9500541

  • 1. A mutation in PDS causes non-syndromic recessive deafness.
    Li XC, Everett LA, Lalwani AK, Desmukh D, Friedman TB, Green ED, Wilcox ER.
    Nat Genet; 1998 Mar; 18(3):215-7. PubMed ID: 9500541
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  • 2. 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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  • 4. Deafness genes.
    Kitamura K, Takahashi K, Tamagawa Y, Noguchi Y, Kuroishikawa Y, Ishikawa K, Hagiwara H.
    J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
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  • 5. Syndromic and non-syndromic deafness, molecular aspects of Pendred syndrome and its reported mutations.
    Shaukat S, Fatima Z, Zehra U, Waqar AB.
    J Ayub Med Coll Abbottabad; 2003 Mar; 15(3):59-64. PubMed ID: 14727345
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  • 8. 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; 10(3):210-2. PubMed ID: 11973626
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  • 9. Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).
    Everett LA, Glaser B, Beck JC, Idol JR, Buchs A, Heyman M, Adawi F, Hazani E, Nassir E, Baxevanis AD, Sheffield VC, Green ED.
    Nat Genet; 1997 Dec; 17(4):411-22. PubMed ID: 9398842
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  • 10. [Identification of two heterozygous mutations in the SLC26A4/PDS gene in a family with Pendred-syndrome].
    Birkenhäger R, Knapp FB, Klenzner T, Aschendorff A, Schipper J.
    Laryngorhinootologie; 2004 Dec; 83(12):831-5. PubMed ID: 15611902
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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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  • 15. Surprising news: a putative sulfate transporter is defective in Pendred's syndrome.
    Rutishauser J, Kopp P.
    Eur J Endocrinol; 1998 Jun 15; 138(6):623-4. PubMed ID: 9678527
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  • 16. DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.
    Delmaghani S, Aghaie A, Compain-Nouaille S, Ataie A, Lemainque A, Zeinali S, Lathrop M, Weil D, Petit C.
    Eur J Hum Genet; 2003 Oct 15; 11(10):816-8. PubMed ID: 14512974
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  • 18. Phenocopies for deafness and goiter development in a large inbred Brazilian kindred with Pendred's syndrome associated with a novel mutation in the PDS gene.
    Kopp P, Arseven OK, Sabacan L, Kotlar T, Dupuis J, Cavaliere H, Santos CL, Jameson JL, Medeiros-Neto G.
    J Clin Endocrinol Metab; 1999 Jan 15; 84(1):336-41. PubMed ID: 9920104
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