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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

170 related items for PubMed ID: 2643315

  • 21. Molecular biological approaches to genetic disorders in prenatal diagnosis.
    Katayama S.
    Early Hum Dev; 1992; 29(1-3):149-53. PubMed ID: 1356752
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  • 22. Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
    Fujishita S, Shibuya N, Niikawa N, Nagataki S.
    Jinrui Idengaku Zasshi; 1991 Dec; 36(4):317-24. PubMed ID: 1811098
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  • 23. Molecular diagnosis of Duchenne muscular dystrophy in Singapore.
    Low PS, Lai PS, Lee WL, Chin SM, Ong HT, Tay JS.
    Ann Acad Med Singap; 1996 Jan; 25(1):84-9. PubMed ID: 8779553
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  • 24. DNA diagnostic tests in Xp21 dystrophy families for prenatal diagnosis.
    Dinçer P, Topaloğlu H, Ayter S.
    Turk J Pediatr; 1998 Jan; 40(3):347-55. PubMed ID: 9763898
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  • 28. [Prenatal diagnosis of Duchenne's muscular dystrophy fetus at risk].
    Hua XY, Xu MH, Lin QD.
    Zhonghua Fu Chan Ke Za Zhi; 1994 Jul; 29(7):408-10, 445. PubMed ID: 8001417
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  • 30. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy.
    Hodgson SV, Bobrow M.
    Br Med Bull; 1989 Jul; 45(3):719-44. PubMed ID: 2688825
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  • 32. Prenatal diagnosis of Duchenne muscular dystrophy: a three-year experience in a rapidly evolving field.
    Bakker E, Bonten EJ, Veenema H, den Dunnen JT, Grootscholten PM, van Ommen GJ, Pearson PL.
    J Inherit Metab Dis; 1989 Jul; 12 Suppl 1():174-90. PubMed ID: 2509804
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  • 33. RFLPs for Duchenne muscular dystrophy cDNA clones 9 and 10.
    Liechti-Gallati S, Schneider V, Mullis P, Moser H.
    Am J Hum Genet; 1990 Jun; 46(6):1090-4. PubMed ID: 1971151
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  • 36. Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphisms.
    Lindlöf M, Kääriäinen H, Davies KE, de la Chapelle A.
    J Med Genet; 1986 Dec; 23(6):560-72. PubMed ID: 2879928
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  • 38. Prenatal diagnosis using deletion studies in Duchenne muscular dystrophy.
    Speer MC, Pericak-Vance MA, Yamaoka LH, Koh J, Hung WY, Gaskell PC, Vance JM, Bartlett RJ, Roses AD.
    Prenat Diagn; 1988 Jul; 8(6):427-37. PubMed ID: 3211845
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  • 39. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF, Harris SG, Tsao CC, Ward PA, Caskey CT.
    Neurology; 1986 Dec; 36(12):1553-62. PubMed ID: 2878392
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  • 40. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL.
    J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
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