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Journal Abstract Search

235 related items for PubMed ID: 16553208

  • 21. [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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  • 22. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP, Pegoraro E, Scacheri P, Burns RG, Taber JW, Weiss L, Spiro A, Blattner P.
    Am J Med Genet; 1996 Jun 28; 63(4):573-80. PubMed ID: 8826437
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  • 25. MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.
    Todorova A, Todorov T, Georgieva B, Lukova M, Guergueltcheva V, Kremensky I, Mitev V.
    Neuromuscul Disord; 2008 Aug 28; 18(8):667-70. PubMed ID: 18653336
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  • 31. Real-time reverse linkage using polar body analysis for preimplantation genetic diagnosis in female carriers of de novo mutations.
    Altarescu G, Eldar-Geva T, Varshower I, Brooks B, Haran EZ, Margalioth EJ, Levy-Lahad E, Renbaum P.
    Hum Reprod; 2009 Dec 28; 24(12):3225-9. PubMed ID: 19687056
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  • 32. 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 28; 9(2):67-80. PubMed ID: 16137182
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  • 34. Rapid and cost effective detection of small mutations in the DMD gene by high resolution melting curve analysis.
    Almomani R, van der Stoep N, Bakker E, den Dunnen JT, Breuning MH, Ginjaar IB.
    Neuromuscul Disord; 2009 Jun 28; 19(6):383-90. PubMed ID: 19409785
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  • 35. 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 28; 52(4):534-9. PubMed ID: 24411039
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  • 39. Analysis of dystrophin gene deletions indicates that the hinge III region of the protein correlates with disease severity.
    Carsana A, Frisso G, Tremolaterra MR, Lanzillo R, Vitale DF, Santoro L, Salvatore F.
    Ann Hum Genet; 2005 May 28; 69(Pt 3):253-9. PubMed ID: 15845029
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  • 40. Molecular diagnosis of Duchenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array-comparative genomic hybridization.
    del Gaudio D, Yang Y, Boggs BA, Schmitt ES, Lee JA, Sahoo T, Pham HT, Wiszniewska J, Chinault AC, Beaudet AL, Eng CM.
    Hum Mutat; 2008 Sep 28; 29(9):1100-7. PubMed ID: 18752307
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