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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

444 related items for PubMed ID: 31250571

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  • 3. Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder.
    Tang F, Ma D, Wang Y, Qiu Y, Liu F, Wang Q, Lu Q, Shi M, Xu L, Liu M, Liang J.
    BMC Med Genet; 2017 Mar 23; 18(1):35. PubMed ID: 28335750
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  • 4. Identification and Clinical Implications of a Novel MYO15A Variant in a Consanguineous Iranian Family by Targeted Exome Sequencing.
    Zarepour N, Koohiyan M, Taghipour-Sheshdeh A, Nemati-Zargaran F, Saki N, Mohammadi-Asl J, Tabatabaiefar MA, Hashemzadeh-Chaleshtori M.
    Audiol Neurootol; 2019 Mar 23; 24(1):25-31. PubMed ID: 30943474
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  • 7. Analysis of the genotype-phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients.
    Fu Y, Huang S, Gao X, Han M, Wang G, Kang D, Yuan Y, Dai P.
    BMC Med Genomics; 2022 Mar 26; 15(1):71. PubMed ID: 35346193
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  • 8. Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss.
    Zheng K, Lin S, Gao J, Chen S, Su J, Liu Z, Duan S.
    BMC Med Genomics; 2024 Jan 02; 17(1):4. PubMed ID: 38167320
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  • 9. Reproductive guidance through prenatal diagnosis and genetic counseling for recessive hereditary hearing loss in high-risk families.
    Deng Y, Sang S, Wen J, Liu Y, Ling J, Chen H, Cai X, Mei L, Chen X, Li M, Li W, Li T, He C, Feng Y.
    Int J Pediatr Otorhinolaryngol; 2018 Dec 02; 115():114-119. PubMed ID: 30368370
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  • 10. Recurrent de novo WFS1 pathogenic variants in Chinese sporadic patients with nonsyndromic sensorineural hearing loss.
    Guan J, Wang H, Lan L, Wu Y, Chen G, Zhao C, Wang D, Wang Q.
    Mol Genet Genomic Med; 2020 Aug 02; 8(8):e1367. PubMed ID: 32567228
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  • 13. Identification of Novel Compound Heterozygous MYO15A Mutations in Two Chinese Families with Autosomal Recessive Nonsyndromic Hearing Loss.
    Wang XH, Xie L, Chen S, Xu K, Bai X, Jin Y, Qiu Y, Liu XZ, Sun Y, Kong WJ.
    Neural Plast; 2021 Aug 02; 2021():9957712. PubMed ID: 34093702
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  • 14. 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 Aug 02; 10(5):e0127879. PubMed ID: 26011067
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  • 17. Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss.
    Mehregan H, Mohseni M, Jalalvand K, Arzhangi S, Nikzat N, Banihashemi S, Kahrizi K, Najmabadi H.
    Int J Pediatr Otorhinolaryngol; 2019 Feb 02; 117():115-126. PubMed ID: 30579064
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