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Journal Abstract Search

370 related items for PubMed ID: 16631122

  • 61. Mitochondrial tRNA(Glu) A14693G variant may modulate the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in a Han Chinese family.
    Ding Y, Li Y, You J, Yang L, Chen B, Lu J, Guan MX.
    J Genet Genomics; 2009 Apr; 36(4):241-50. PubMed ID: 19376484
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  • 63. Isolated hearing loss associated with T7511C mutation in mitochondrial DNA.
    Yamasoba T, Tsukuda K, Suzuki M.
    Acta Otolaryngol Suppl; 2007 Dec; (559):13-8. PubMed ID: 18340555
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  • 64. [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; 34(2):77-80. PubMed ID: 12764852
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  • 65. 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; 8(1):1-7. PubMed ID: 17136632
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  • 66. Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation.
    Kobayashi K, Oguchi T, Asamura K, Miyagawa M, Horai S, Abe S, Usami S.
    Auris Nasus Larynx; 2005 Jun; 32(2):119-24. PubMed ID: 15917167
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  • 67. Phenotype of DFNA11: a nonsyndromic hearing loss caused by a myosin VIIA mutation.
    Tamagawa Y, Ishikawa K, Ishikawa K, Ishida T, Kitamura K, Makino S, Tsuru T, Ichimura K.
    Laryngoscope; 2002 Feb; 112(2):292-7. PubMed ID: 11889386
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  • 69. [Large-scale screening of mtDNA A1555G mutation in China and its significance in prevention of aminoglycoside antibiotic induced deafness].
    Liu X, Dai P, Huang DL, Yuan HJ, Li WM, Cao JY, Yu F, Zhang RN, Lin HY, Zhu XH, He Y, Yu YJ, Yao K.
    Zhonghua Yi Xue Za Zhi; 2006 May 23; 86(19):1318-22. PubMed ID: 16796900
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  • 70. 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 23; 15(11):1145-55. PubMed ID: 17637808
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  • 73. Mitochondrial syndromic sensorineural hearing loss.
    Forli F, Passetti S, Mancuso M, Seccia V, Siciliano G, Nesti C, Berrettini S.
    Biosci Rep; 2007 Jun 23; 27(1-3):113-23. PubMed ID: 17487579
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  • 74. Co-segregation of the T1095C with the A1555G mutation of the mitochondrial 12S rRNA gene in a patient with non-syndromic hearing loss.
    Dai D, Lu Y, Chen Z, Wei Q, Cao X, Xing G.
    Biochem Biophys Res Commun; 2008 Dec 26; 377(4):1152-5. PubMed ID: 18983818
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  • 75. 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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  • 76. Carriers of the Usher syndrome type IB: is audiometric identification possible?
    Wagenaar M, Snik AF, Kimberling WJ, Cremers CW.
    Am J Otol; 1996 Nov 28; 17(6):853-8. PubMed ID: 8915413
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  • 78. Phylogenetic analysis of mitochondrial DNA in Japanese pedigrees of sensorineural hearing loss associated with the A1555G mutation.
    Abe S, Usami S, Shinkawa H, Weston MD, Overbeck LD, Hoover DM, Kenyon JB, Horai S, Kimberling WJ.
    Eur J Hum Genet; 1998 Nov 28; 6(6):563-9. PubMed ID: 9887373
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