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Journal Abstract Search

267 related items for PubMed ID: 16137182

  • 1. 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; 9(2):67-80. PubMed ID: 16137182
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  • 3. Direct deletion analysis in two Duchenne muscular dystrophy symptomatic females using polymorphic dinucleotide (CA)n loci within the dystrophin gene.
    Giliberto F, Ferreiro V, Dalamón V, Surace E, Cotignola J, Esperante S, Borelina D, Baranzini S, Szijan I.
    J Biochem Mol Biol; 2003 Mar 31; 36(2):179-84. PubMed ID: 12689516
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  • 4. Carrier detection in non-deletional Duchenne/Becker muscular dystrophy families using polymorphic dinucleotide (CA) repeat loci of dystrophin gene.
    Chaturvedi LS, Srivastava S, Mukherjee M, Mittal RD, Phadke SR, Pradhan S, Mittal B.
    Indian J Med Res; 2001 Jan 31; 113():19-25. PubMed ID: 11280167
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  • 6. [Carrier detection of Duchenne/Becker muscular dystrophy by analysis of STRs loci linked to the gene of dystrophin in Venezuelan families].
    Delgado-Luengo WN, Borjas-Fuentes L, Zabala-Fernández W, Fernández-Salgado E, Solís-Añez E, Chávez C, Martínez-Basalo C, González-Ferrer S, Rojas-Atencio A, Morales-Machin A, Peña J, Pineda-Bernal L, González R, Miranda LE, Delgado-Luengo J, Hernández ML, Chacín JA, Quintero M.
    Invest Clin; 2002 Dec 31; 43(4):239-54. PubMed ID: 12520997
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  • 7. Molecular diagnosis of Duchenne/Becker muscular dystrophy by polymerase chain reaction and microsatellite analysis.
    Kim UK, Chae JJ, Lee SH, Lee CC, Namkoong Y.
    Mol Cells; 2002 Jun 30; 13(3):385-8. PubMed ID: 12132577
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  • 8. 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 30; 52(4):534-9. PubMed ID: 24411039
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  • 12. [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 30; 31(3):338-43. PubMed ID: 24928015
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  • 14. Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy.
    Dinh LT, Tran VK, Luong LH, Le PT, Nguyen AD, Thi Nguyen BS, Chi DV, Tran TH, Bui TH, Van Ta T, Nguyen DH.
    Taiwan J Obstet Gynecol; 2019 Sep 30; 58(5):645-649. PubMed ID: 31542086
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  • 15. Carrier detection of Duchenne/Becker muscular dystrophy by using fluorescent linkage analysis in Taiwan.
    Lee CC, Wu MC, Wu JY, Li TC, Tsai FJ, Tsai CH.
    Acta Paediatr Taiwan; 2000 Sep 30; 41(2):69-74. PubMed ID: 10927942
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  • 16. Intragenic DNA polymorphism analysis of DMD/BMD dystrophy gene for carrier and prenatal diagnosis in 60 Iranian healthy individuals.
    Zamani M, Salahshour V, Kollaee A, Zamani GR, Sheidai M, Mohammadi M, Ghaffarpor M.
    Int J Neurosci; 2011 Oct 30; 121(10):551-6. PubMed ID: 21774744
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  • 18. [Mutation analysis and prenatal diagnosis of families affected with Duchenne and Becker muscular dystrophy].
    Wang WJ, Zhu HY, Zhu RF, Yang Y, Zhu XY, Duan HL, Zhang Y, Wu X.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Feb 30; 30(1):45-8. PubMed ID: 23450478
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  • 19. Detection of germline mosaicism in two Duchenne muscular dystrophy families using polymorphic dinucleotide (CA)n repeat loci within the dystrophin gene.
    Ferreiro V, Szijan I, Giliberto F.
    Mol Diagn; 2004 Feb 30; 8(2):115-21. PubMed ID: 15527326
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  • 20. Genetic analysis of 62 Chinese families with Duchenne muscular dystrophy and strategies of prenatal diagnosis in a single center.
    Zhang J, Ma D, Liu G, Wang Y, Liu A, Li L, Luo C, Hu P, Xu Z.
    BMC Med Genet; 2019 Nov 14; 20(1):180. PubMed ID: 31727011
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