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Journal Abstract Search

192 related items for PubMed ID: 6745920

  • 1. 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; 67(1):115-9. PubMed ID: 6745920
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  • 2. Duchenne muscular dystrophy in a female with a translocation involving Xp21.
    Nevin NC, Hughes AE, Calwell M, Lim JH.
    J Med Genet; 1986 Apr; 23(2):171-3. PubMed ID: 3712394
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  • 3. 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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  • 6. 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 Jul; 71(4):370-1. PubMed ID: 4077054
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  • 8. Duchenne muscular dystrophy in a girl with an (X;15) translocation.
    Ribeiro MC, Melaragno MI, Schmidt B, Brunoni D, Gabbai AA, Hackel C.
    Am J Med Genet; 1986 Oct; 25(2):231-6. PubMed ID: 3777020
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  • 9. 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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  • 11. Turner's syndrome and Duchenne muscular dystrophy in a girl with an X; autosome translocation.
    Bjerglund Nielsen L, Nielsen IM.
    Ann Genet; 1984 Dec; 27(3):173-7. PubMed ID: 6334482
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  • 12. 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 Dec; 8(6):619-23. PubMed ID: 3826553
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  • 13. 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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  • 16. [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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  • 18. Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy.
    Bodrug SE, Roberson JR, Weiss L, Ray PN, Worton RG, Van Dyke DL.
    J Med Genet; 1990 Jul; 27(7):426-32. PubMed ID: 2395160
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  • 20. Prenatal evaluation of a de novo X;9 translocation.
    Feldman B, Kramer RL, Ebrahim SA, Wolff DJ, Evans MI.
    Am J Med Genet; 1999 Aug 27; 85(5):476-8. PubMed ID: 10405445
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