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Journal Abstract Search

128 related items for PubMed ID: 24006325

  • 1. Advances in genetic diagnostics for hereditary hearing loss.
    Idan N, Brownstein Z, Shivatzki S, Avraham KB.
    J Basic Clin Physiol Pharmacol; 2013; 24(3):165-70. PubMed ID: 24006325
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  • 2. Genetic diagnostics of early childhood hearing loss: better testing with next-generation DNA sequencing.
    Sommen M, Van Camp G.
    B-ENT; 2013; Suppl 21():51-6. PubMed ID: 24383223
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  • 3. [Hereditary hearing loss: genetic counselling].
    Cabanillas Farpón R, Cadiñanos Bañales J.
    Acta Otorrinolaringol Esp; 2012; 63(3):218-29. PubMed ID: 21514544
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  • 4. Navigating genetic diagnostics in patients with hearing loss.
    Sloan-Heggen CM, Smith RJ.
    Curr Opin Pediatr; 2016 Dec; 28(6):705-712. PubMed ID: 27552069
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  • 7. Molecular diagnostics for hereditary hearing loss in children.
    Sommen M, Wuyts W, Van Camp G.
    Expert Rev Mol Diagn; 2017 Aug; 17(8):751-760. PubMed ID: 28593790
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  • 8. Genetic testing as part of the early hearing detection and intervention (EHDI) process.
    Schimmenti LA, Martinez A, Fox M, Crandall B, Shapiro N, Telatar M, Sininger Y, Grody WW, Palmer CG.
    Genet Med; 2004 Aug; 6(6):521-5. PubMed ID: 15545749
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  • 10. Developments in molecular genetic diagnostics: an update for the pediatric epilepsy specialist.
    Pong AW, Pal DK, Chung WK.
    Pediatr Neurol; 2011 May; 44(5):317-27. PubMed ID: 21481738
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  • 11. [Application of next generation sequencing in gene identification and genetic diagnosis of hereditary hearing loss].
    Huijun Y, Yu L.
    Yi Chuan; 2014 Nov; 36(11):1112-20. PubMed ID: 25567869
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  • 12. Performance evaluation of the next-generation sequencing approach for molecular diagnosis of hereditary hearing loss.
    Sivakumaran TA, Husami A, Kissell D, Zhang W, Keddache M, Black AP, Tinkle BT, Greinwald JH, Zhang K.
    Otolaryngol Head Neck Surg; 2013 Jun; 148(6):1007-16. PubMed ID: 23525850
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  • 13. Extensive and rapid screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss.
    Kato T, Nishigaki Y, Noguchi Y, Ueno H, Hosoya H, Ito T, Kimura Y, Kitamura K, Tanaka M.
    J Hum Genet; 2010 Mar; 55(3):147-54. PubMed ID: 20111055
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  • 16. A rapid automatic processing platform for bead label-assisted microarray analysis: application for genetic hearing-loss mutation detection.
    Zhu J, Song X, Xiang G, Feng Z, Guo H, Mei D, Zhang G, Wang D, Mitchelson K, Xing W, Cheng J.
    J Lab Autom; 2014 Apr; 19(2):144-52. PubMed ID: 23975388
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  • 20. [Attitudes towards prenatal diagnosis of deafness among parents to children with cochlear implants].
    Thorsen A, Devantier L, Ovesen T.
    Ugeskr Laeger; 2009 Apr 20; 171(17):1387-91. PubMed ID: 19413935
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