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Journal Abstract Search

203 related items for PubMed ID: 2895584

  • 1.
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  • 2. [Carrier detection and gene analysis in a Duchenne muscular dystrophy family].
    Lu FM.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1990 Aug; 23(4):231-3, 255. PubMed ID: 1979269
    [Abstract] [Full Text] [Related]

  • 3. Germline mosaicism and Duchenne muscular dystrophy mutations.
    Bakker E, Van Broeckhoven C, Bonten EJ, van de Vooren MJ, Veenema H, Van Hul W, Van Ommen GJ, Vandenberghe A, Pearson PL.
    Nature; 1990 Aug; 329(6139):554-6. PubMed ID: 2889144
    [Abstract] [Full Text] [Related]

  • 4. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N.
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
    [Abstract] [Full Text] [Related]

  • 5. Mental retardation locus in Xp21 chromosome microdeletion.
    Fries MH, Lebo RV, Schonberg SA, Golabi M, Seltzer WK, Gitelman SE, Golbus MS.
    Am J Med Genet; 1993 Jun 01; 46(4):363-8. PubMed ID: 8357005
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  • 7. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF, Francke U, Bonilla E, Martucci G, Schmidt B, Salviati G, Rubin M.
    Am J Med Genet; 1989 Feb 01; 32(2):268-73. PubMed ID: 2648829
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  • 10. Xp21/autosome translocations. Case report and risk for Duchenne muscular dystrophy.
    Holden JJ, Smith A, MacLeod PM, Masotti R, Duncan AM.
    Clin Genet; 1986 Jun 01; 29(6):516-22. PubMed ID: 3742857
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  • 12. Update on the molecular genetics of Duchenne muscular dystrophy.
    Siddique T, Bartlett R, Pericak-Vance M, Yamaoka L, Koh J, Chen J, Hung WY, Kandt R, Roses AD.
    Aust Paediatr J; 1988 Jun 01; 24 Suppl 1():9-14. PubMed ID: 3060079
    [Abstract] [Full Text] [Related]

  • 13. Familial deletion in Becker type muscular dystrophy within the pXJ region.
    Liechti-Gallati S, Braga S, Hirsiger H, Moser H.
    Hum Genet; 1987 Nov 01; 77(3):267-8. PubMed ID: 2890571
    [Abstract] [Full Text] [Related]

  • 14. Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.
    den Dunnen JT, Bakker E, Breteler EG, Pearson PL, van Ommen GJ.
    Nature; 1987 Nov 01; 329(6140):640-2. PubMed ID: 2889148
    [Abstract] [Full Text] [Related]

  • 15. Duchenne muscular dystrophy in monozygotic twins: deletion of 5' fragments of the gene.
    Ionasescu VV, Searby CC, Ionasescu R, Patil S.
    Am J Med Genet; 1989 May 01; 33(1):113-6. PubMed ID: 2750778
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  • 17. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
    Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM.
    Nature; 1989 May 01; 323(6089):646-50. PubMed ID: 3773991
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  • 19. Somatic mosaicism at the Duchenne locus.
    Lebo RV, Olney RK, Golbus MS.
    Am J Med Genet; 1990 Oct 01; 37(2):187-90. PubMed ID: 1978985
    [Abstract] [Full Text] [Related]

  • 20. Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals: deletion detection and familial diagnosis.
    Patiño A, Narbona J, García-Delgado M.
    Am J Med Genet; 1995 Nov 06; 59(2):182-7. PubMed ID: 8588583
    [Abstract] [Full Text] [Related]

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