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PUBMED FOR HANDHELDS

Journal Abstract Search

138 related items for PubMed ID: 2564818

  • 21. Detection of dystrophin deletion carriers using FISH analysis.
    Calvano S, Memeo E, Piemontese MR, Melchionda S, Bisceglia L, Gasparini P, Zelante L.
    Clin Genet; 1997 Jul; 52(1):17-22. PubMed ID: 9272708
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  • 22. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW, Papp AC, Snyder PJ, Mendell JR.
    Muscle Nerve; 1992 Aug; 15(8):960-3. PubMed ID: 1353862
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  • 27. Carrier detection and gene analysis of Duchenne muscular dystrophy.
    Pearson PL, van Ommen GJ, Bakker E.
    Cold Spring Harb Symp Quant Biol; 1986 Aug; 51 Pt 1():353-8. PubMed ID: 2884063
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  • 28. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
    Thompson MW, Ray PN, Belfall B, Duff C, Logan C, Oss I, Worton RG.
    J Med Genet; 1986 Dec; 23(6):548-55. PubMed ID: 2879926
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  • 30. Analysis of RFLPs and DNA deletions in the Chinese Duchenne muscular dystrophy gene.
    Zeng YT, Chen MJ, Ren ZR, Qui XK, Huang SZ.
    J Med Genet; 1991 Mar; 28(3):167-70. PubMed ID: 1675685
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  • 32. Isolation of probes detecting restriction fragment length polymorphisms from X chromosome-specific libraries: potential use for diagnosis of Duchenne muscular dystrophy.
    Hofker MH, Wapenaar MC, Goor N, Bakker E, van Ommen GJ, Pearson PL.
    Hum Genet; 1985 Mar; 70(2):148-56. PubMed ID: 2989153
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  • 33. High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling.
    Alcántara MA, Villarreal MT, Del Castillo V, Gutiérrez G, Saldaña Y, Maulen I, Lee R, Macías M, Orozco L.
    Clin Genet; 1999 May; 55(5):376-80. PubMed ID: 10422811
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  • 34. The significance of different types of information in calculating the probability that a female relative of a Duchenne muscular dystrophy patient is a carrier.
    ten Kate LP, Offringa PJ.
    Clin Genet; 1981 Oct; 20(4):281-8. PubMed ID: 7333021
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  • 35. Carrier detection in Duchenne muscular dystrophy.
    Fitzsimmons JS, McLachlan JI, Reeves WG, Marriott DW, Woolfson AM, Mayhew J.
    J Med Genet; 1980 Jun; 17(3):165-9. PubMed ID: 7401126
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  • 36. 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; 29(3):713-26. PubMed ID: 2897793
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  • 37. Effect of exercise on serum creatine kinase in carriers of Duchenne muscular dystrophy.
    Gaines RF, Pueschel SM, Sassaman EA, Driscoll JL.
    J Med Genet; 1982 Feb; 19(1):4-7. PubMed ID: 7069744
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  • 38. Diagnosis of DMD carrier status in a family with no known affected males.
    Muntoni F, Mateddu A, Cau M, Congiu R, Puddu R, Cossu P, Cao A, Melis MA.
    Dev Med Child Neurol; 1993 Jan; 35(1):70-3. PubMed ID: 8095479
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  • 39. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC, Gedeon AK, Haan EA, Sheffield LJ, White SJ, Bates LJ, Robertson EF, Sutherland GR.
    Aust Paediatr J; 1988 Jan; 24 Suppl 1():92-7. PubMed ID: 3202740
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  • 40. Detection of Duchenne and Becker muscular dystrophy carriers by quantitative multiplex polymerase chain reaction analysis.
    Ioannou P, Christopoulos G, Panayides K, Kleanthous M, Middleton L.
    Neurology; 1992 Sep; 42(9):1783-90. PubMed ID: 1513470
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