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Journal Abstract Search

376 related items for PubMed ID: 32860223

  • 1.
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  • 2. Spectrum of Genes for Non-GJB2-Related Non-Syndromic Hearing Loss in the Russian Population Revealed by a Targeted Deafness Gene Panel.
    Shatokhina O, Galeeva N, Stepanova A, Markova T, Lalayants M, Alekseeva N, Tavarkiladze G, Markova T, Bessonova L, Petukhova M, Guseva D, Anisimova I, Polyakov A, Ryzhkova O, Bliznetz E.
    Int J Mol Sci; 2022 Dec 12; 23(24):. PubMed ID: 36555390
    [Abstract] [Full Text] [Related]

  • 3. Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta-analysis.
    Aliazami F, Gilani S, Farhud D, Naraghi M, Afshari M, Eslami M.
    Int J Pediatr Otorhinolaryngol; 2023 May 12; 168():111512. PubMed ID: 37086676
    [Abstract] [Full Text] [Related]

  • 4. Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene.
    Čada Z, Šafka Brožková D, Balatková Z, Plevová P, Rašková D, Laštůvková J, Černý R, Bandúrová V, Koucký V, Hrubá S, Komarc M, Jenčík J, Poisson Marková S, Plzák J, Kluh J, Seeman P.
    Eur Arch Otorhinolaryngol; 2019 Dec 12; 276(12):3353-3358. PubMed ID: 31552524
    [Abstract] [Full Text] [Related]

  • 5. Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia.
    Sansović I, Meašić AM, Bobinec A, Morožin Pohovski L, Odak L, Vulin K, Lozić B, Kero M, Huljev Frković S, Pušeljić S.
    Croat Med J; 2024 Jun 13; 65(3):198-208. PubMed ID: 38868966
    [Abstract] [Full Text] [Related]

  • 6. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
    Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T.
    Orphanet J Rare Dis; 2013 Oct 28; 8():172. PubMed ID: 24164807
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  • 8. Genetic profiles of non-syndromic severe-profound hearing loss in Chinese Hans by whole-exome sequencing.
    Liu Y, Tan M, Cai L, Lv L, Chen Q, Chen W, Yang H, Xu Y.
    Gene; 2022 Apr 20; 819():146258. PubMed ID: 35114279
    [Abstract] [Full Text] [Related]

  • 9. Whole-exome sequencing identifies rare pathogenic and candidate variants in sporadic Chinese Han deaf patients.
    Zou S, Mei X, Yang W, Zhu R, Yang T, Hu H.
    Clin Genet; 2020 Feb 20; 97(2):352-356. PubMed ID: 31486067
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  • 11. Genetic Predisposition to Sporadic Congenital Hearing Loss in a Pediatric Population.
    Jung J, Lee JS, Cho KJ, Yu S, Yoon JH, Yung Gee H, Choi JY.
    Sci Rep; 2017 Apr 06; 7():45973. PubMed ID: 28383030
    [Abstract] [Full Text] [Related]

  • 12. Identification of novel variants in MYO15A, OTOF, and RDX with hearing loss by next-generation sequencing.
    Bai X, Nian S, Feng L, Ruan Q, Luo X, Wu M, Yan Z.
    Mol Genet Genomic Med; 2019 Aug 06; 7(8):e808. PubMed ID: 31250571
    [Abstract] [Full Text] [Related]

  • 13. Genetic spectrum of autosomal recessive non-syndromic hearing loss in Pakistani families.
    Shafique S, Siddiqi S, Schraders M, Oostrik J, Ayub H, Bilal A, Ajmal M, Seco CZ, Strom TM, Mansoor A, Mazhar K, Shah ST, Hussain A, Azam M, Kremer H, Qamar R.
    PLoS One; 2014 Aug 06; 9(6):e100146. PubMed ID: 24949729
    [Abstract] [Full Text] [Related]

  • 14. Molecular genetic landscape of hereditary hearing loss in Pakistan.
    Naz S.
    Hum Genet; 2022 Apr 06; 141(3-4):633-648. PubMed ID: 34308486
    [Abstract] [Full Text] [Related]

  • 15. STRC Deletion is a Frequent Cause of Slight to Moderate Congenital Hearing Impairment in the Czech Republic.
    Plevova P, Paprskarova M, Tvrda P, Turska P, Slavkovsky R, Mrazkova E.
    Otol Neurotol; 2017 Dec 06; 38(10):e393-e400. PubMed ID: 28984810
    [Abstract] [Full Text] [Related]

  • 16. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
    Liang P, Chen F, Wang S, Li Q, Li W, Wang J, Chen J, Zha D.
    Int J Pediatr Otorhinolaryngol; 2021 Sep 06; 148():110817. PubMed ID: 34265623
    [Abstract] [Full Text] [Related]

  • 17. Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing.
    Hutchin T, Coy NN, Conlon H, Telford E, Bromelow K, Blaydon D, Taylor G, Coghill E, Brown S, Trembath R, Liu XZ, Bitner-Glindzicz M, Mueller R.
    Clin Genet; 2005 Dec 06; 68(6):506-12. PubMed ID: 16283880
    [Abstract] [Full Text] [Related]

  • 18. Variant analysis of 92 Chinese Han families with hearing loss.
    Jin X, Huang S, An L, Zhang C, Dai P, Gao H, Ma X.
    BMC Med Genomics; 2022 Jan 21; 15(1):12. PubMed ID: 35062939
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