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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

252 related items for PubMed ID: 36833326

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  • 2. Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden.
    Adadey SM, Wonkam-Tingang E, Twumasi Aboagye E, Nayo-Gyan DW, Boatemaa Ansong M, Quaye O, Awandare GA, Wonkam A.
    Life (Basel); 2020 Oct 28; 10(11):. PubMed ID: 33126609
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  • 5. GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairment.
    Grønskov K, Larsen LA, Rendtorff ND, Parving A, Nørgaard-Pedersen B, Brøndum-Nielsen K.
    Genet Test; 2004 Oct 28; 8(2):181-4. PubMed ID: 15345117
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  • 7. Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.
    Santos RL, Wajid M, Pham TL, Hussan J, Ali G, Ahmad W, Leal SM.
    Clin Genet; 2005 Jan 28; 67(1):61-8. PubMed ID: 15617550
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  • 9. Molecular genetic landscape of hereditary hearing loss in Pakistan.
    Naz S.
    Hum Genet; 2022 Apr 28; 141(3-4):633-648. PubMed ID: 34308486
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  • 11. Overinterpretation of high throughput sequencing data in medical genetics: first evidence against TMPRSS3/GJB2 digenic inheritance of hearing loss.
    Ołdak M, Lechowicz U, Pollak A, Oziębło D, Skarżyński H.
    J Transl Med; 2019 Aug 14; 17(1):269. PubMed ID: 31412945
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  • 12. Frequency of GJB2 mutations, GJB6-D13S1830 and GJB6-D13S1854 deletions among patients with non-syndromic hearing loss from the central region of Iran.
    Naddafnia H, Noormohammadi Z, Irani S, Salahshoorifar I.
    Mol Genet Genomic Med; 2019 Jul 14; 7(7):e00780. PubMed ID: 31162818
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  • 13. Connexin 26 35delG does not represent a mutational hotspot.
    Rothrock CR, Murgia A, Sartorato EL, Leonardi E, Wei S, Lebeis SL, Yu LE, Elfenbein JL, Fisher RA, Friderici KH.
    Hum Genet; 2003 Jul 14; 113(1):18-23. PubMed ID: 12684873
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  • 15. Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations.
    Aboagye ET, Adadey SM, Esoh K, Jonas M, de Kock C, Amenga-Etego L, Awandare GA, Wonkam A.
    Biology (Basel); 2022 Mar 21; 11(3):. PubMed ID: 35336849
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  • 19. Mutation in gap and tight junctions in patients with non-syndromic hearing loss.
    Belguith H, Tlili A, Dhouib H, Ben Rebeh I, Lahmar I, Charfeddine I, Driss N, Ghorbel A, Ayadi H, Masmoudi S.
    Biochem Biophys Res Commun; 2009 Jul 17; 385(1):1-5. PubMed ID: 19254696
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