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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 4077054

  • 1. High-resolution banding study of an X/4 translocation in a female with Duchenne muscular dystrophy.
    Saito F, Tonomura A, Kimura S, Misugi N, Sugita H.
    Hum Genet; 1985; 71(4):370-1. PubMed ID: 4077054
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  • 2. Duchenne muscular dystrophy (DMD) in a female with an X/autosome translocation: further evidence that the DMD locus is at Xp21.
    Jacobs PA, Hunt PA, Mayer M, Bart RD.
    Am J Hum Genet; 1981 Jul; 33(4):513-8. PubMed ID: 7258185
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  • 4. Clinical features in a girl with Duchenne muscular dystrophy with an X-autosome translocation; (X;4)(p21;q26).
    Kimura S, Mitsuda T, Misugi N, Saito F, Tonomura A, Sugita H.
    Brain Dev; 1986 Jul; 8(6):619-23. PubMed ID: 3826553
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  • 6. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome.
    Verellen-Dumoulin C, Freund M, De Meyer R, Laterre C, Frédéric J, Thompson MW, Markovic VD, Worton RG.
    Hum Genet; 1984 Jul; 67(1):115-9. PubMed ID: 6745920
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  • 9. [Duchenne muscular dystrophy in a girl with chromosomal translocation].
    Werneck LC, Lemos SM, Magdalena N.
    Arq Neuropsiquiatr; 1988 Dec; 46(4):401-5. PubMed ID: 3245772
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  • 10. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.
    Lindenbaum RH, Clarke G, Patel C, Moncrieff M, Hughes JT.
    J Med Genet; 1979 Oct; 16(5):389-92. PubMed ID: 513085
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  • 11. Further evidence for Xp21 location of Duchenne muscular dystrophy (DMD) locus: X;9 translocation in a female with DMD.
    Emanuel BS, Zackai EH, Tucker SH.
    J Med Genet; 1983 Dec; 20(6):461-3. PubMed ID: 6655672
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  • 15. Mapping of 12 translocation breakpoints in the Xp21 region with respect to the locus for Duchenne muscular dystrophy.
    Boyd Y, Cockburn D, Holt S, Munro E, Van Ommen GJ, Gillard B, Affara N, Ferguson-Smith M, Craig I.
    Cytogenet Cell Genet; 1988 Dec; 48(1):28-34. PubMed ID: 3180845
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  • 16. Molecular analysis of a constitutional X-autosome translocation in a female with muscular dystrophy.
    Bodrug SE, Ray PN, Gonzalez IL, Schmickel RD, Sylvester JE, Worton RG.
    Science; 1987 Sep 25; 237(4822):1620-4. PubMed ID: 3629260
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  • 17. De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy.
    Chelly J, Marlhens F, Le Marec B, Jeanpierre M, Lambert M, Hamard G, Dutrillaux B, Kaplan JC.
    Hum Genet; 1986 Oct 25; 74(2):193-6. PubMed ID: 2876949
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