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Pubmed for Handhelds

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Journal Abstract Search

201 related items for PubMed ID: 31620164

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  • 4. Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana.
    Adadey SM, Tingang Wonkam E, Twumasi Aboagye E, Quansah D, Asante-Poku A, Quaye O, Amedofu GK, Awandare GA, Wonkam A.
    Genes (Basel); 2020 Jan 27; 11(2):. PubMed ID: 32012697
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  • 5. 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 Jan 27; 23(5-6):184-189. PubMed ID: 33302283
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  • 8. No evidence for clinical utility in investigating the connexin genes GJB2, GJB6 and GJA1 in non-syndromic hearing loss in black Africans.
    Wonkam A, Bosch J, Noubiap JJ, Lebeko K, Makubalo N, Dandara C.
    S Afr Med J; 2015 Jan 27; 105(1):23-6. PubMed ID: 26046157
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  • 11. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
    Abidi O, Boulouiz R, Nahili H, Ridal M, Alami MN, Tlili A, Rouba H, Masmoudi S, Chafik A, Hassar M, Barakat A.
    Int J Pediatr Otorhinolaryngol; 2007 Aug 27; 71(8):1239-45. PubMed ID: 17553572
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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 27; 7(7):e00780. PubMed ID: 31162818
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  • 13. 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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  • 16. Absence of GJB6 mutations in Indian patients with non-syndromic hearing loss.
    Bhalla S, Sharma R, Khandelwal G, Panda NK, Khullar M.
    Int J Pediatr Otorhinolaryngol; 2011 Mar 28; 75(3):356-9. PubMed ID: 21227513
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  • 17. GJB3/GJB6 screening in GJB2 carriers with idiopathic hearing loss: Is it necessary?
    Chen K, Wu X, Zong L, Jiang H.
    J Clin Lab Anal; 2018 Nov 28; 32(9):e22592. PubMed ID: 29926981
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  • 20. Analyses of del(GJB6-D13S1830) and del(GJB6-D13S1834) deletions in a large cohort with hearing loss: Caveats to interpretation of molecular test results in multiplex families.
    Pandya A, O'Brien A, Kovasala M, Bademci G, Tekin M, Arnos KS.
    Mol Genet Genomic Med; 2020 Apr 28; 8(4):e1171. PubMed ID: 32067424
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