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Journal Abstract Search

340 related items for PubMed ID: 3014348

  • 21. Mild and severe muscular dystrophy associated with deletions in Xp21 of the human X chromosome.
    Davies KE, Smith TJ, Bundey S, Read AP, Flint T, Bell M, Speer A.
    J Med Genet; 1988 Jan; 25(1):9-13. PubMed ID: 3162536
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  • 22. Localization of the region homologous to the Duchenne muscular dystrophy locus on the mouse X chromosome.
    Heilig R, Lemaire C, Mandel JL, Dandolo L, Amar L, Avner P.
    Nature; 1988 Jan; 328(6126):168-70. PubMed ID: 3600794
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  • 24. DGGE-based whole-gene mutation scanning of the dystrophin gene in Duchenne and Becker muscular dystrophy patients.
    Hofstra RM, Mulder IM, Vossen R, de Koning-Gans PA, Kraak M, Ginjaar IB, van der Hout AH, Bakker E, Buys CH, van Ommen GJ, van Essen AJ, den Dunnen JT.
    Hum Mutat; 2004 Jan; 23(1):57-66. PubMed ID: 14695533
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  • 25. DNA deletions in mild and severe Becker muscular dystrophy.
    Hart KA, Hodgson S, Walker A, Cole CG, Johnson L, Dubowitz V, Bobrow M.
    Hum Genet; 1987 Mar; 75(3):281-5. PubMed ID: 3030926
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  • 28. Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment.
    Monaco AP, Bertelson CJ, Middlesworth W, Colletti CA, Aldridge J, Fischbeck KH, Bartlett R, Pericak-Vance MA, Roses AD, Kunkel LM.
    Nature; 1987 Mar; 316(6031):842-5. PubMed ID: 2993910
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  • 35. A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male.
    Darras BT, Francke U.
    Nature; 1987 Mar; 329(6139):556-8. PubMed ID: 2889145
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  • 36. Further studies of gene deletions that cause Duchenne and Becker muscular dystrophies.
    Forrest SM, Cross GS, Flint T, Speer A, Robson KJ, Davies KE.
    Genomics; 1988 Feb; 2(2):109-14. PubMed ID: 3410474
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  • 38. Deletion analysis of Duchenne muscular dystrophy.
    Erdem H, Ayter S, Ozgüç M, Topçu M, Topaloğlu H, Renda Y.
    Turk J Pediatr; 1993 Feb; 35(1):15-21. PubMed ID: 8236513
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  • 39. Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy.
    Hodgson S, Hart K, Abbs S, Heckmatt J, Rodillo E, Bobrow M, Dubowitz V.
    J Med Genet; 1989 Nov; 26(11):682-93. PubMed ID: 2585468
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  • 40. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S, Shukin RJ, McGillivray BC, Ray PN, Worton RG.
    Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584
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