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Journal Abstract Search

532 related items for PubMed ID: 23767834

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  • 2. Genetic etiology study of four Chinese families with two nonsyndromic deaf children in succession by targeted next-generation sequencing.
    Xiao C, Liu S, Wang H, Ding Y, Chen Y, Liu H.
    Mol Genet Genomic Med; 2021 Apr; 9(4):e1634. PubMed ID: 33638616
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  • 4. Targeted next-generation sequencing in Uyghur families with non-syndromic sensorineural hearing loss.
    Chen Y, Wang Z, Wang Z, Chen D, Chai Y, Pang X, Sun L, Wang X, Yang T, Wu H.
    PLoS One; 2015 Apr; 10(5):e0127879. PubMed ID: 26011067
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  • 5. Molecular epidemiology of Chinese Han deaf patients with bi-allelic and mono-allelic GJB2 mutations.
    Yu X, Lin Y, Xu J, Che T, Li L, Yang T, Wu H.
    Orphanet J Rare Dis; 2020 Jan 28; 15(1):29. PubMed ID: 31992338
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  • 8. 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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  • 9. Whole exome sequencing identifies new causative mutations in Tunisian families with non-syndromic deafness.
    Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, Boespflug OT, Besbes G, Abdelhak S, Petit C.
    PLoS One; 2014 Oct 28; 9(6):e99797. PubMed ID: 24926664
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  • 17. [Analysis of the hereditary etiology of 336 patients with non-syndromic sensorineural hearing loss from Ningxia Hui Autonomous Region of China].
    Wang YL, Zhu YM, Liu XW, Xu BC, Guo YF, Wang QJ.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Sep 28; 47(9):760-3. PubMed ID: 23141447
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