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Journal Abstract Search

285 related items for PubMed ID: 22830166

  • 21. Identification of female carriers for Duchenne and Becker muscular dystrophies using a FISH-based approach.
    Ligon AH, Kashork CD, Richards CS, Shaffer LG.
    Eur J Hum Genet; 2000 Apr; 8(4):293-8. PubMed ID: 10854113
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  • 24. Prenatal diagnosis of Duchenne muscular dystrophy.
    Maheshwari M, Vijaya R, Kabra M, Arora S, Shastri SS, Deka D, Kriplani A, Menon PS.
    Natl Med J India; 2000 Apr; 13(3):129-31. PubMed ID: 11558111
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  • 26. 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; 113():19-25. PubMed ID: 11280167
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  • 28. Carrier detection in Duchenne and Becker muscular dystrophy Argentine families.
    Baranzini SE, Giliberto F, Dalamon V, Barreiro C, García-Erro M, Grippo J, Szijan I.
    Clin Genet; 1998 Dec; 54(6):503-11. PubMed ID: 9894797
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  • 32. [Changes of serum creatine kinase levels in children with Duchenne muscular dystrophy].
    Sun SC, Peng YS, He JB.
    Zhongguo Dang Dai Er Ke Za Zhi; 2008 Feb; 10(1):35-7. PubMed ID: 18289468
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  • 35. A larger spectrum of intragenic short tandem repeats improves linkage analysis and localization of intragenic recombination detection in the dystrophin gene: an analysis of 93 families from southern Italy.
    Carsana A, Frisso G, Tremolaterra MR, Ricci E, De Rasmo D, Salvatore F.
    J Mol Diagn; 2007 Feb; 9(1):64-9. PubMed ID: 17251337
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  • 36. DUCHEN: an interactive computer program for calculating heterozygosity (carrier) risks in X-linked recessive lethal diseases, and its application in Duchenne muscular dystrophy.
    Andrews DF, Brasher PM, Manchester KE, Percy ME, Rusk AC, Soltan HC, Trueman DW.
    Am J Med Genet; 1986 Oct; 25(2):211-8. PubMed ID: 3777018
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  • 38. Prenatal molecular diagnosis of Duchenne and Becker muscular dystrophy.
    Li Q, Li SY, Hu DG, Sun XF, Chen DJ, Zhang C, Jiang WY.
    Beijing Da Xue Xue Bao Yi Xue Ban; 2006 Feb 18; 38(1):53-6. PubMed ID: 16415967
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  • 39. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
    Darras BT, Koenig M, Kunkel LM, Francke U.
    Am J Med Genet; 1988 Mar 18; 29(3):713-26. PubMed ID: 2897793
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  • 40. [Detection of genomic duplications and deletions of the DMD gene in affected males and female carriers by using mutiplex ligation-dependent probe amplification].
    Shen BC, Zhang C, Sun XF, Zhang HM, Li SY.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Aug 18; 24(4):460-3. PubMed ID: 17680544
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