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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

291 related items for PubMed ID: 33126609

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  • 3. Hearing loss in Africa: current genetic profile.
    Adadey SM, Wonkam-Tingang E, Aboagye ET, Quaye O, Awandare GA, Wonkam A.
    Hum Genet; 2022 Apr; 141(3-4):505-517. PubMed ID: 34609590
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  • 4. GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana.
    Adadey SM, Manyisa N, Mnika K, de Kock C, Nembaware V, Quaye O, Amedofu GK, Awandare GA, Wonkam A.
    Front Genet; 2019 Apr; 10():841. PubMed ID: 31620164
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  • 8. Molecular genetics of hearing impairment due to mutations in gap junction genes encoding beta connexins.
    Rabionet R, Gasparini P, Estivill X.
    Hum Mutat; 2000 Sep; 16(3):190-202. PubMed ID: 10980526
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  • 9. Screening for GJB2-R143W-Associated Hearing Impairment: Implications for Health Policy and Practice in Ghana.
    Adadey SM, Quaye O, Amedofu GK, Awandare GA, Wonkam A.
    Public Health Genomics; 2020 Sep; 23(5-6):184-189. PubMed ID: 33302283
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  • 11. Whole exome sequencing identifies rare coding variants in novel human-mouse ortholog genes in African individuals diagnosed with non-syndromic hearing impairment.
    Oluwole OG, Esoh KK, Wonkam-Tingang E, Manyisa N, Noubiap JJ, Chimusa ER, Wonkam A.
    Exp Biol Med (Maywood); 2021 Jan; 246(2):197-206. PubMed ID: 32996353
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  • 14. 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; 7(7):e00780. PubMed ID: 31162818
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  • 16. [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?].
    Birkenhäger R, Zimmer AJ, Maier W, Schipper J.
    Laryngorhinootologie; 2006 Mar; 85(3):191-6. PubMed ID: 16547895
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  • 18. Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment.
    Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M.
    Biochem Biophys Res Commun; 2009 Jul 31; 385(3):445-8. PubMed ID: 19465004
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  • 19. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.
    Gravina LP, Foncuberta ME, Prieto ME, Garrido J, Barreiro C, Chertkoff L.
    Int J Pediatr Otorhinolaryngol; 2010 Mar 31; 74(3):250-4. PubMed ID: 20022641
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