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Journal Abstract Search

62 related items for PubMed ID: 21811982

  • 1. [Clinical significance of large-scale screening of A1555G mutation of mitochondria DNA for neonates].
    Cai J, Luo CQ, Xie JS, Wu WQ, Geng Q, Xu ZY, Hao Y, Xu XX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):414-6. PubMed ID: 21811982
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  • 3. Mutation screening of the mitochondrial genome using denaturing high-performance liquid chromatography.
    Biggin A, Henke R, Bennetts B, Thorburn DR, Christodoulou J.
    Mol Genet Metab; 2005 Jan; 84(1):61-74. PubMed ID: 15639196
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  • 4. [A novel method of detecting mitochondrial C1494T and A1555G mutations by using the base-quenched probe technique in a single PCR assay].
    ZHENG L, LUO GH, ZHANG J, ZHANG XY, XU N.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Apr; 47(4):326-9. PubMed ID: 22800354
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  • 7. Clinical applications of denaturing high-performance liquid chromatography-based genotyping.
    Danielson PB, Shelton RJ, LaBerge GS.
    Croat Med J; 2003 Aug; 44(4):447-54. PubMed ID: 12950149
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  • 8. Rapid screening of the entire mitochondrial DNA for low-level heteroplasmic mutations.
    Meierhofer D, Mayr JA, Ebner S, Sperl W, Kofler B.
    Mitochondrion; 2005 Aug; 5(4):282-96. PubMed ID: 16050991
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  • 11. Noninvasive Test for Mitochondrial DNA A1555G Mutation Associated with Deafness.
    Fan W, Zhu Y, Tang X, Xue L.
    Clin Lab; 2017 Jan 01; 63(1):127-131. PubMed ID: 28164482
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  • 12. [Mutation analysis of 12S rRNA and tRNA-Ser(UCN) genes in a large Chinese family with maternally inherited nonsyndromic hearing loss by intermarriage].
    Shu AL, Ji BH, Qin W, Feng GY, Nie YZ, Liu T, He L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun 01; 23(3):303-5. PubMed ID: 16767669
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  • 15. [Influence of DNA polymerases on mutation screening of denaturing high-performance liquid chromatography].
    Liu MR, Pan KF, Wang Y, Lu YY.
    Ai Zheng; 2002 Oct 01; 21(10):1160-3. PubMed ID: 12508666
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  • 18. Hearing loss due to the mitochondrial A1555G mutation in Italian families.
    Casano RA, Bykhovskaya Y, Johnson DF, Hamon M, Torricelli F, Bigozzi M, Fischel-Ghodsian N.
    Am J Med Genet; 1998 Oct 12; 79(5):388-91. PubMed ID: 9779807
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