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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

216 related items for PubMed ID: 22484064

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  • 24. [Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment].
    Schade G, Kothe C, Ruge G, Hess M, Meyer CG.
    Laryngorhinootologie; 2003 Jun; 82(6):397-401. PubMed ID: 12851846
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  • 29. Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant.
    Gazzaz B, Weil D, Raïs L, Akhyat O, Azeddoug H, Nadifi S.
    Hear Res; 2005 Dec; 210(1-2):80-4. PubMed ID: 16243461
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  • 30. Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population.
    Kokotas H, Van Laer L, Grigoriadou M, Iliadou V, Economides J, Pomoni S, Pampanos A, Eleftheriades N, Ferekidou E, Korres S, Giannoulia-Karantana A, Van Camp G, Petersen MB.
    Am J Med Genet A; 2008 Nov 15; 146A(22):2879-84. PubMed ID: 18925674
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  • 34. The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population.
    Mikstiene V, Jakaitiene A, Byckova J, Gradauskiene E, Preiksaitiene E, Burnyte B, Tumiene B, Matuleviciene A, Ambrozaityte L, Uktveryte I, Domarkiene I, Rancelis T, Cimbalistiene L, Lesinskas E, Kucinskas V, Utkus A.
    BMC Genet; 2016 Feb 19; 17():45. PubMed ID: 26896187
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  • 38. Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates.
    Hochman JB, Stockley TL, Shipp D, Lin VY, Chen JM, Nedzelski JM.
    Otol Neurotol; 2010 Aug 19; 31(6):919-22. PubMed ID: 20601923
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