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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

252 related items for PubMed ID: 31552524

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  • 10. [Hearing loss due to mutations or lack of the gene coding protein stereocillin].
    Markova TG, Alekseeva NN, Mironovich OL, Bliznets EA, Lalayants MR, Polyakov AV, Tavartkiladze GA.
    Vestn Otorinolaringol; 2020; 85(2):14-20. PubMed ID: 32476383
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  • 11. Prevalence and Characteristics of STRC Gene Mutations (DFNB16): A Systematic Review and Meta-Analysis.
    Han S, Zhang D, Guo Y, Fu Z, Guan G.
    Front Genet; 2021; 12():707845. PubMed ID: 34621290
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  • 15. [The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances].
    Lalaiants MR, Markova TG, Bakhshinian VV, Bliznets EA, Poliakov AV, Tavartikiladze GA.
    Vestn Otorinolaringol; 2014; (2):37-43. PubMed ID: 24781170
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  • 18. GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methods.
    Bartsch O, Vatter A, Zechner U, Kohlschmidt N, Wetzig C, Baumgart A, Nospes S, Haaf T, Keilmann A.
    Audiol Neurootol; 2010; 15(6):375-82. PubMed ID: 20234132
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  • 20. Novel Pathogenic Variants in the Gene Encoding Stereocilin (STRC) Causing Non-Syndromic Moderate Hearing Loss in Spanish and Argentinean Subjects.
    Domínguez-Ruiz M, Ruiz-Palmero L, Buonfiglio PI, García-Vaquero I, Gómez-Rosas E, Goñi M, Villamar M, Morín M, Moreno-Pelayo MA, Elgoyhen AB, Del Castillo FJ, Dalamón V, Del Castillo I.
    Biomedicines; 2023 Oct 31; 11(11):. PubMed ID: 38001944
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