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PUBMED FOR HANDHELDS

Journal Abstract Search


300 related items for PubMed ID: 23770805

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  • 3. Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.
    Muskett JA, Chattaraj P, Heneghan JF, Reimold FR, Shmukler BE, Brewer CC, King KA, Zalewski CK, Shawker TH, Butman JA, Kenna MA, Chien WW, Alper SL, Griffith AJ.
    Laryngoscope; 2016 Jul; 126(7):E240-7. PubMed ID: 26485571
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  • 6. Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.
    Ben Said M, Dhouib H, BenZina Z, Ghorbel A, Moreno F, Masmoudi S, Ayadi H, Hmani-Aifa M.
    Int J Pediatr Otorhinolaryngol; 2012 Jun; 76(6):832-6. PubMed ID: 22429511
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  • 12. Novel and recurrent MYO7A mutations in Usher syndrome type 1 and type 2.
    Rong W, Chen X, Zhao K, Liu Y, Liu X, Ha S, Liu W, Kang X, Sheng X, Zhao C.
    PLoS One; 2014 Jun; 9(5):e97808. PubMed ID: 24831256
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  • 13. Allelic hierarchy of CDH23 mutations causing non-syndromic deafness DFNB12 or Usher syndrome USH1D in compound heterozygotes.
    Schultz JM, Bhatti R, Madeo AC, Turriff A, Muskett JA, Zalewski CK, King KA, Ahmed ZM, Riazuddin S, Ahmad N, Hussain Z, Qasim M, Kahn SN, Meltzer MR, Liu XZ, Munisamy M, Ghosh M, Rehm HL, Tsilou ET, Griffith AJ, Zein WM, Brewer CC, Riazuddin S, Friedman TB.
    J Med Genet; 2011 Nov; 48(11):767-75. PubMed ID: 21940737
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  • 16. Mutation profile of the CDH23 gene in 56 probands with Usher syndrome type I.
    Oshima A, Jaijo T, Aller E, Millan JM, Carney C, Usami S, Moller C, Kimberling WJ.
    Hum Mutat; 2008 Jun; 29(6):E37-46. PubMed ID: 18429043
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  • 20. A novel mutation in the MYO7A gene is associated with Usher syndrome type 1 in a Chinese family.
    He X, Peng Q, Li S, Zhu P, Wu C, Rao C, Lin J, Lu X.
    Int J Pediatr Otorhinolaryngol; 2017 Aug; 99():40-43. PubMed ID: 28688563
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