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Journal Abstract Search

214 related items for PubMed ID: 19586859

  • 1. [Prenatal diagnosis of Duchenne and Becker muscular dystrophy by multiplex ligation-dependent probe amplification].
    Wang Q, Jin CL, Lin CK, Cui WT, Ma HW, Wu YY.
    Yi Chuan; 2009 Jun; 31(6):600-4. PubMed ID: 19586859
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  • 3. [Genetic diagnosis of Duchenne/Becker muscular dystrophy by MLPA].
    Zhang Y, Liu X, He R, Ma H, Zhao Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Jun; 31(3):338-43. PubMed ID: 24928015
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  • 6. Gene diagnosis for nine Chinese patients with DMD/BMD by multiplex ligation-dependent probe amplification and prenatal diagnosis for one of them.
    Wu Y, Yin G, Fu K, Wu D, Zhai Q, Du H, Huang Z, Niu Y.
    J Clin Lab Anal; 2009 Jun; 23(6):380-6. PubMed ID: 19927354
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  • 7. Rapid method for targeted prenatal diagnosis of Duchenne muscular dystrophy in Vietnam.
    Ta MH, Tran TH, Do NH, Pham le AT, Bui TH, Ta VT, Tran VK.
    Taiwan J Obstet Gynecol; 2013 Dec; 52(4):534-9. PubMed ID: 24411039
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  • 10. The role of polymorphic short tandem (CA)n repeat loci segregation analysis in the detection of Duchenne muscular dystrophy carriers and prenatal diagnosis.
    Ferreiro V, Giliberto F, Francipane L, Szijan I.
    Mol Diagn; 2005 Dec; 9(2):67-80. PubMed ID: 16137182
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  • 11. Characteristics of dystrophin gene mutations among Chinese patients as revealed by multiplex ligation-dependent probe amplification.
    Wang Q, Li-Ling J, Lin C, Wu Y, Sun K, Ma H, Jin C.
    Genet Test Mol Biomarkers; 2009 Feb; 13(1):23-30. PubMed ID: 19309270
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  • 12. [Genotype, phenotype analysis and follow-up study on patients with Duchenne/Becker muscular dystrophy].
    Zhang YZ, Xiong H, Wang XZ, Wang S, Luo J, Wang JM, Jiang YW, Chang XZ, Pan H, Qi JG, Li WZ, Yuan Y, Wu XR.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2010 Dec 18; 42(6):661-6. PubMed ID: 21170096
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  • 13. [Efficiency of multiplex ligation-dependent probe amplification combined with short tandem repeat linkage analysis for the prenatal diagnosis for Duchenne muscular dystrophy].
    Li T, Wu D, Hou QF, Wang L, Guo QN, Kang B, Liu HY, Yang K, Ding XB, Liao SX.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb 18; 30(1):40-4. PubMed ID: 23450477
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  • 14. Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne muscular dystrophy (DMD) gene mutation analysis.
    Murugan S, Chandramohan A, Lakshmi BR.
    Indian J Med Res; 2010 Sep 18; 132():303-11. PubMed ID: 20847377
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  • 15. [Mutation analysis and prenatal diagnosis for 50 pedigrees affected with Duchenne/Becker muscular dystrophy].
    Li H, Xu C, Mao Y, Lu J, Xiang Y, Xu X, Tang S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2018 Apr 10; 35(2):169-174. PubMed ID: 29652985
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  • 16. [Mutation analysis and prenatal diagnosis of sporadic DMD/BMD families].
    Zhu HY, Li J, Yang Y, Wu X, Zhu XY, Zhu RF, Zhang Y, Duan HL, Hu YL.
    Zhonghua Yi Xue Za Zhi; 2009 Jul 07; 89(25):1753-6. PubMed ID: 19862979
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  • 17. Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).
    Gatta V, Scarciolla O, Gaspari AR, Palka C, De Angelis MV, Di Muzio A, Guanciali-Franchi P, Calabrese G, Uncini A, Stuppia L.
    Hum Genet; 2005 Jun 07; 117(1):92-8. PubMed ID: 15841391
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