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Journal Abstract Search

149 related items for PubMed ID: 19959154

  • 1. [Pendred's syndrome: a cause of goiter associated with deafness].
    Vázquez AG, Montesinos IG, Jiménez AM, García JA, García JG, Hernández JA.
    Endocrinol Nutr; 2009 Oct; 56(8):428-30. PubMed ID: 19959154
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  • 2. Pendred's syndrome: identification of the genetic defect a century after its recognition.
    Kopp P.
    Thyroid; 1999 Jan; 9(1):65-9. PubMed ID: 10037079
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  • 4. A novel mutation in the pendrin gene associated with Pendred's syndrome.
    Bogazzi F, Raggi F, Ultimieri F, Campomori A, Cosci C, Berrettini S, Neri E, La Rocca R, Ronca G, Martino E, Bartalena L.
    Clin Endocrinol (Oxf); 2000 Mar; 52(3):279-85. PubMed ID: 10718825
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  • 6. Genetics and phenomics of Pendred syndrome.
    Bizhanova A, Kopp P.
    Mol Cell Endocrinol; 2010 Jun 30; 322(1-2):83-90. PubMed ID: 20298745
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  • 9. Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome.
    Gausden E, Armour JA, Coyle B, Coffey R, Hochberg Z, Pembrey M, Britton KE, Grossman A, Reardon W, Trembath R.
    Clin Endocrinol (Oxf); 1996 Apr 30; 44(4):441-6. PubMed ID: 8706311
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  • 20. Screening of SLC26A4 (PDS) gene in Pendred's syndrome: a large spectrum of mutations in France and phenotypic heterogeneity.
    Blons H, Feldmann D, Duval V, Messaz O, Denoyelle F, Loundon N, Sergout-Allaoui A, Houang M, Duriez F, Lacombe D, Delobel B, Leman J, Catros H, Journel H, Drouin-Garraud V, Obstoy MF, Toutain A, Oden S, Toublanc JE, Couderc R, Petit C, Garabédian EN, Marlin S.
    Clin Genet; 2004 Oct 30; 66(4):333-40. PubMed ID: 15355436
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