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Pubmed for Handhelds

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Journal Abstract Search

203 related items for PubMed ID: 11748854

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  • 6. Analysis of the SLC26A4 gene in patients with Pendred syndrome in Taiwan.
    Lai CC, Chiu CY, Shiao AS, Tso YC, Wu YC, Tu TY, Jap TS.
    Metabolism; 2007 Sep; 56(9):1279-84. PubMed ID: 17697873
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  • 10. Pendred syndrome and iodide transport in the thyroid.
    Kopp P, Pesce L, Solis-S JC.
    Trends Endocrinol Metab; 2008 Sep; 19(7):260-8. PubMed ID: 18692402
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  • 11. The Pendred syndrome gene encodes a chloride-iodide transport protein.
    Scott DA, Wang R, Kreman TM, Sheffield VC, Karniski LP.
    Nat Genet; 1999 Apr; 21(4):440-3. PubMed ID: 10192399
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  • 14. Identification of a novel mutation in the SLC26A4 gene in an Italian with fluctuating sensorineural hearing loss.
    Cama E, Alemanno MS, Bellacchio E, Santarelli R, Carella M, Zelante L, Palladino T, Inches I, di Paola F, Arslan E, Melchionda S.
    Int J Pediatr Otorhinolaryngol; 2009 Oct; 73(10):1458-63. PubMed ID: 19615760
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  • 15. 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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  • 17. Distribution and frequencies of PDS (SLC26A4) mutations in Pendred syndrome and nonsyndromic hearing loss associated with enlarged vestibular aqueduct: a unique spectrum of mutations in Japanese.
    Tsukamoto K, Suzuki H, Harada D, Namba A, Abe S, Usami S.
    Eur J Hum Genet; 2003 Dec 30; 11(12):916-22. PubMed ID: 14508505
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  • 19. 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 30; 84(1):336-41. PubMed ID: 9920104
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