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Journal Abstract Search

63 related items for PubMed ID: 9798335

  • 21. Somatic mosaicism at the Duchenne locus.
    Lebo RV, Olney RK, Golbus MS.
    Am J Med Genet; 1990 Oct; 37(2):187-90. PubMed ID: 1978985
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  • 25. Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis.
    LeRoy BS, Uhrhammer NA, Steere KJ, Boehm CD, King RA, Rich SS, Williams PP, Smith SA, de Martinville B.
    Am J Med Genet; 1988 Nov; 31(3):709-21. PubMed ID: 2906525
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  • 26. Identify female carriers and de novo mutations in deletional Duchenne/Becker muscular dystrophy families.
    Zhu HY, Wu LQ, Liang DS, Pan Q, Xia JH.
    Yi Chuan Xue Bao; 2006 Mar; 33(3):206-12. PubMed ID: 16553208
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  • 27. The value of deletion analysis for carrier detection in Duchenne muscular dystrophy (DMD).
    Bejjani B, Finn P, Milunsky A, Amos J.
    Clin Genet; 1991 Apr; 39(4):245-52. PubMed ID: 2070545
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  • 29. Making the most of multiple measurements in estimating carrier probability in Duchenne muscular dystrophy: the Bayesian incorporation of repeated measurements using logistic discrimination.
    Percy ME, Andrews DF, Brasher PM, Rusk AC.
    Am J Med Genet; 1987 Apr; 26(4):851-61. PubMed ID: 3591827
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  • 30. 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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  • 31. [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; 43(4):239-54. PubMed ID: 12520997
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  • 32. Duchenne/Becker muscular dystrophy carrier detection using quantitative PCR and fluorescence-based strategies.
    Mansfield ES, Robertson JM, Lebo RV, Lucero MY, Mayrand PE, Rappaport E, Parrella T, Sartore M, Surrey S, Fortina P.
    Am J Med Genet; 1993 Dec 15; 48(4):200-8. PubMed ID: 7510932
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  • 36. Detection of Duchenne muscular dystrophy carriers by dosage analysis using the DMD cDNA clone 8.
    Mao YP, Cremer M.
    Hum Genet; 1989 Jan 15; 81(2):193-5. PubMed ID: 2912889
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  • 38. A small in-frame deletion within the protease domain of muscle-specific calpain, p94 causes early-onset limb-girdle muscular dystrophy 2A.
    Häffner K, Speer A, Hübner C, Voit T, Oexle K.
    Hum Mutat; 1998 Jan 15; Suppl 1():S298-300. PubMed ID: 9452114
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  • 40. The genetic status of mothers of isolated cases of Duchenne muscular dystrophy.
    Lane RJ, Robinow M, Roses AD.
    J Med Genet; 1983 Feb 15; 20(1):1-11. PubMed ID: 6842530
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