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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

276 related items for PubMed ID: 12768662

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  • 23. Audiological features and mitochondrial DNA sequence in a large family carrying mitochondrial A1555G mutation without use of aminoglycoside.
    Matsunaga T, Kumanomido H, Shiroma M, Goto Y, Usami S.
    Ann Otol Rhinol Laryngol; 2005 Feb; 114(2):153-60. PubMed ID: 15757197
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  • 26. Whole mitochondrial genome screening in maternally inherited non-syndromic hearing impairment using a microarray resequencing mitochondrial DNA chip.
    Lévêque M, Marlin S, Jonard L, Procaccio V, Reynier P, Amati-Bonneau P, Baulande S, Pierron D, Lacombe D, Duriez F, Francannet C, Mom T, Journel H, Catros H, Drouin-Garraud V, Obstoy MF, Dollfus H, Eliot MM, Faivre L, Duvillard C, Couderc R, Garabedian EN, Petit C, Feldmann D, Denoyelle F.
    Eur J Hum Genet; 2007 Nov; 15(11):1145-55. PubMed ID: 17637808
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  • 27. Clinical evaluation and mitochondrial DNA sequence analysis in two Chinese families with aminoglycoside-induced and non-syndromic hearing loss.
    Zhao L, Wang Q, Qian Y, Li R, Cao J, Hart LC, Zhai S, Han D, Young WY, Guan MX.
    Biochem Biophys Res Commun; 2005 Oct 28; 336(3):967-73. PubMed ID: 16168391
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  • 28. Hearing assessment in pre-school children with speech delay.
    Psillas G, Psifidis A, Antoniadou-Hitoglou M, Kouloulas A.
    Auris Nasus Larynx; 2006 Sep 28; 33(3):259-63. PubMed ID: 16420975
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  • 29. [Audiologic analysis of a family with nonsyndromic genetic progressive sensorineural hearing loss].
    Ni D, Dan H, Mo J.
    Zhonghua Er Bi Yan Hou Ke Za Zhi; 1999 Apr 28; 34(2):77-80. PubMed ID: 12764852
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  • 30. Audiological evaluation of affected members from a Dutch DFNA8/12 (TECTA) family.
    Plantinga RF, Cremers CW, Huygen PL, Kunst HP, Bosman AJ.
    J Assoc Res Otolaryngol; 2007 Mar 28; 8(1):1-7. PubMed ID: 17136632
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  • 31. Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.
    Verhoeven K, Ensink RJ, Tiranti V, Huygen PL, Johnson DF, Schatteman I, Van Laer L, Verstreken M, Van de Heyning P, Fischel-Ghodsian N, Zeviani M, Cremers CW, Willems PJ, Van Camp G.
    Eur J Hum Genet; 1999 Jan 28; 7(1):45-51. PubMed ID: 10094190
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  • 32. [Family history, clinical features, and molecular characterization of a patient with autosomal recessive non-syndromic hearing loss].
    Düzcan F, Wollnik B, Tepeli E, Ardiç FN, Uyguner O, Bağci H.
    Kulak Burun Bogaz Ihtis Derg; 2003 Sep 28; 11(3):85-8. PubMed ID: 14699249
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  • 34. Cochlear implantation in a patient with profound hearing loss with the A1555G mitochondrial DNA mutation and no history of aminoglycoside exposure.
    Ulubil SA, Furze AD, Angeli SI.
    J Laryngol Otol; 2006 Mar 28; 120(3):230-2. PubMed ID: 16359140
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  • 39. Cochlear origin of hearing loss in MELAS syndrome.
    Sue CM, Lipsett LJ, Crimmins DS, Tsang CS, Boyages SC, Presgrave CM, Gibson WP, Byrne E, Morris JG.
    Ann Neurol; 1998 Mar 28; 43(3):350-9. PubMed ID: 9506552
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  • 40. [Screening for mitochondrial DNA mutation in two pedigrees with nonsyndromic inherited sensorineural hearing loss].
    Li W, Han D, Yuan H, Wang Y, Cao J, Yang W, Jiang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2002 Feb 28; 19(1):64-7. PubMed ID: 11836692
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