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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

229 related items for PubMed ID: 32864763

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  • 4. Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.
    Zarepour N, Koohiyan M, Taghipour-Sheshdeh A, Nemati-Zargaran F, Saki N, Mohammadi-Asl J, Tabatabaiefar MA, Hashemzadeh-Chaleshtori M.
    Audiol Neurootol; 2019; 24(1):25-31. PubMed ID: 30943474
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  • 7. Novel MYO15A variants are associated with hearing loss in the two Iranian pedigrees.
    Khatami S, Askari M, Bahreini F, Hashemzadeh-Chaleshtori M, Hematian S, Asgharzade S.
    BMC Med Genet; 2020 Nov 18; 21(1):226. PubMed ID: 33208113
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  • 10. A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing.
    Asgharzade S, Tabatabaiefar MA, Mohammadi-Asl J, Chaleshtori MH.
    Int J Pediatr Otorhinolaryngol; 2018 May 18; 108():8-11. PubMed ID: 29605370
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  • 11. A Novel Pathogenic Variant in the CABP2 Gene Causes Severe Nonsyndromic Hearing Loss in a Consanguineous Iranian Family.
    Koohiyan M, Noori-Daloii MR, Hashemzadeh-Chaleshtori M, Salehi M, Abtahi H, Tabatabaiefar MA.
    Audiol Neurootol; 2019 May 18; 24(5):258-263. PubMed ID: 31661684
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  • 12. Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis.
    Aliazami F, Gilani S, Farhud D, Naraghi M, Afshari M, Eslami M.
    Int J Pediatr Otorhinolaryngol; 2023 May 18; 168():111512. PubMed ID: 37086676
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  • 13. Targeted next-generation sequencing of deafness genes in hearing-impaired individuals uncovers informative mutations.
    Vona B, Müller T, Nanda I, Neuner C, Hofrichter MA, Schröder J, Bartsch O, Läßig A, Keilmann A, Schraven S, Kraus F, Shehata-Dieler W, Haaf T.
    Genet Med; 2014 Dec 18; 16(12):945-53. PubMed ID: 24875298
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  • 15. Screening of OTOF mutations in Iran: a novel mutation and review.
    Mahdieh N, Shirkavand A, Rabbani B, Tekin M, Akbari B, Akbari MT, Zeinali S.
    Int J Pediatr Otorhinolaryngol; 2012 Nov 18; 76(11):1610-5. PubMed ID: 22906306
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  • 18. TMPRSS3 mutations in autosomal recessive nonsyndromic hearing loss.
    Battelino S, Klancar G, Kovac J, Battelino T, Trebusak Podkrajsek K.
    Eur Arch Otorhinolaryngol; 2016 May 18; 273(5):1151-4. PubMed ID: 26036852
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  • 19. Comprehensive Analysis of Deafness Genes in Families with Autosomal Recessive Nonsyndromic Hearing Loss.
    Atik T, Onay H, Aykut A, Bademci G, Kirazli T, Tekin M, Ozkinay F.
    PLoS One; 2015 May 18; 10(11):e0142154. PubMed ID: 26561413
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