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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

225 related items for PubMed ID: 33638616

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  • 6. Targeted next-generation sequencing of deaf patients from Southwestern China.
    Li Y, Su J, Zhang J, Pei J, Li D, Zhang Y, Li J, Chen M, Zhu B.
    Mol Genet Genomic Med; 2021 Apr; 9(4):e1660. PubMed ID: 33724713
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  • 10. Comparative study of mutation spectrums of MT-RNR1 m.1555A>G, GJB2, and SLC26A4 between familial and sporadic patients with nonsyndromic sensorineural hearing loss in Chinese Han.
    Li Q, Ji Y, Han B, Zong L, Lan L, Zhao Y, Wang H, Wang D, Wang Q.
    Chin Med J (Engl); 2014 Apr; 127(18):3233-7. PubMed ID: 25266519
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  • 13. Genetic Etiology Study of Ten Chinese Families with Nonsyndromic Hearing Loss.
    Hu S, Sun F, Zhang J, Tang Y, Qiu J, Wang Z, Zhang L.
    Neural Plast; 2018 Apr; 2018():4920980. PubMed ID: 30123251
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  • 14. Mutation analysis of seven consanguineous Uyghur families with non-syndromic deafness.
    Wang ZT, Chen Y, Chen DY, Chai YC, Pang XH, Sun LH, Wang XW, Yang T, Wu H.
    Int J Pediatr Otorhinolaryngol; 2014 Sep; 78(9):1513-6. PubMed ID: 25015771
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  • 15. Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss.
    Jiang H, Chen J, Shan XJ, Li Y, He JG, Yang BB.
    Mol Med Rep; 2014 Jul; 10(1):379-86. PubMed ID: 24737404
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  • 16. Clinical and genetic study of 12 Chinese Han families with nonsyndromic deafness.
    Wu D, Huang W, Xu Z, Li S, Zhang J, Chen X, Tang Y, Qiu J, Wang Z, Duan X, Zhang L.
    Mol Genet Genomic Med; 2020 Apr; 8(4):e1177. PubMed ID: 32048449
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  • 19. 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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