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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

209 related items for PubMed ID: 32996353

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  • 2. Whole exome sequencing reveals pathogenic variants in MYO3A, MYO15A and COL9A3 and differential frequencies in ancestral alleles in hearing impairment genes among individuals from Cameroon.
    Wonkam A, Manyisa N, Bope CD, Dandara C, Chimusa ER.
    Hum Mol Genet; 2021 Feb 04; 29(23):3729-3743. PubMed ID: 33078831
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  • 5. Bi-Allelic Novel Variants in CLIC5 Identified in a Cameroonian Multiplex Family with Non-Syndromic Hearing Impairment.
    Wonkam-Tingang E, Schrauwen I, Esoh KK, Bharadwaj T, Nouel-Saied LM, Acharya A, Nasir A, Adadey SM, Mowla S, Leal SM, Wonkam A.
    Genes (Basel); 2020 Oct 23; 11(11):. PubMed ID: 33114113
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  • 8. 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 23; 32(9):e22592. PubMed ID: 29926981
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  • 13. Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma.
    Schrauwen I, Melegh BI, Chakchouk I, Acharya A, Nasir A, Poston A, Cornejo-Sanchez DM, Szabo Z, Karosi T, Bene J, Melegh B, Leal SM.
    Eur J Hum Genet; 2019 Jun 23; 27(6):869-878. PubMed ID: 30872814
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  • 14. 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 Jun 23; 8(2):181-4. PubMed ID: 15345117
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  • 15. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.
    Sarmadi A, Nasrniya S, Narrei S, Nouri Z, Abtahi H, Tabatabaiefar MA.
    Mol Biol Rep; 2020 Jul 23; 47(7):5355-5364. PubMed ID: 32623615
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  • 17. A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana.
    Adadey SM, Aboagye ET, Esoh K, Acharya A, Bharadwaj T, Lin NS, Amenga-Etego L, Awandare GA, Schrauwen I, Leal SM, Wonkam A.
    BMC Med Genomics; 2022 Nov 10; 15(1):237. PubMed ID: 36357908
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  • 18. Genetics of hearing loss in Africans: use of next generation sequencing is the best way forward.
    Lebeko K, Bosch J, Noubiap JJ, Dandara C, Wonkam A.
    Pan Afr Med J; 2015 Nov 10; 20():383. PubMed ID: 26185573
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  • 19. Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment.
    Aboagye ET, Adadey SM, Wonkam-Tingang E, Amenga-Etego L, Awandare GA, Wonkam A.
    Genes (Basel); 2023 Feb 03; 14(2):. PubMed ID: 36833326
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  • 20. 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 03; 26(1):2-18. PubMed ID: 35041532
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