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Pubmed for Handhelds

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Journal Abstract Search

291 related items for PubMed ID: 33126609

  • 21. 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; 67(1):61-8. PubMed ID: 15617550
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  • 23. Hearing Impairment Overview in Africa: the Case of Cameroon.
    Wonkam Tingang E, Noubiap JJ, F Fokouo JV, Oluwole OG, Nguefack S, Chimusa ER, Wonkam A.
    Genes (Basel); 2020 Feb 22; 11(2):. PubMed ID: 32098311
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  • 25. Connexin 26 (GJB2) Mutations Associated with Non-Syndromic Hearing Loss (NSHL).
    Mishra S, Pandey H, Srivastava P, Mandal K, Phadke SR.
    Indian J Pediatr; 2018 Dec 22; 85(12):1061-1066. PubMed ID: 29542069
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  • 27. Prevalence of DFNB1 mutations in Slovak patients with non-syndromic hearing loss.
    Minárik G, Tretinárová D, Szemes T, Kádasi L.
    Int J Pediatr Otorhinolaryngol; 2012 Mar 22; 76(3):400-3. PubMed ID: 22281373
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  • 29. [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 22; 82(6):397-401. PubMed ID: 12851846
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  • 31. Frequencies of gap- and tight-junction mutations in Turkish families with autosomal-recessive non-syndromic hearing loss.
    Uyguner O, Emiroglu M, Uzumcu A, Hafiz G, Ghanbari A, Baserer N, Yuksel-Apak M, Wollnik B.
    Clin Genet; 2003 Jul 22; 64(1):65-9. PubMed ID: 12791041
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  • 33. Absence of GJB3 and GJB6 mutations in Moroccan familial and sporadic patients with autosomal recessive non-syndromic deafness.
    Nahili H, Ridal M, Boulouiz R, Abidi O, Imken L, Rouba H, Alami MN, Chafik A, Hassar M, Barakat A.
    Int J Pediatr Otorhinolaryngol; 2008 Nov 22; 72(11):1633-6. PubMed ID: 18809214
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  • 34. GJB2 mutations in patients with nonsyndromic hearing loss from Croatia.
    Sansović I, Knezević J, Musani V, Seeman P, Barisić I, Pavelić J.
    Genet Test Mol Biomarkers; 2009 Oct 22; 13(5):693-9. PubMed ID: 19814620
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  • 36. GJB2-associated hearing loss undetected by hearing screening of newborns.
    Minami SB, Mutai H, Nakano A, Arimoto Y, Taiji H, Morimoto N, Sakata H, Adachi N, Masuda S, Sakamoto H, Yoshida H, Tanaka F, Morita N, Sugiuchi T, Kaga K, Matsunaga T.
    Gene; 2013 Dec 10; 532(1):41-5. PubMed ID: 24013081
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  • 39. Hearing Impairment in South Africa and the Lessons Learned for Planetary Health Genomics: A Systematic Review.
    Manyisa N, Adadey SM, Wonkam-Tingang E, Yalcouye A, Wonkam A.
    OMICS; 2022 Jan 10; 26(1):2-18. PubMed ID: 35041532
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  • 40. GJB4 and GJC3 variants in non-syndromic hearing impairment in Ghana.
    Adadey SM, Esoh KK, Quaye O, Amedofu GK, Awandare GA, Wonkam A.
    Exp Biol Med (Maywood); 2020 Sep 10; 245(15):1355-1367. PubMed ID: 32524838
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