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Journal Abstract Search

276 related items for PubMed ID: 513085

  • 1. 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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  • 3. Translocation (X;6) in a female with Duchenne muscular dystrophy: implications for the localisation of the DMD locus.
    Zatz M, Vianna-Morgante AM, Campos P, Diament AJ.
    J Med Genet; 1981 Dec; 18(6):442-7. PubMed ID: 7334502
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  • 4. [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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  • 6. 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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  • 7. 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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  • 8. Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy.
    Kean VM, Macleod HL, Thompson MW, Ray PN, Verellen-Dumoulin C, Worton RG.
    J Med Genet; 1986 Dec; 23(6):491-3. PubMed ID: 2879921
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  • 9. 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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  • 10. 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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  • 11. 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 Sep 25; 67(1):115-9. PubMed ID: 6745920
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  • 12. 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 Sep 25; 71(4):370-1. PubMed ID: 4077054
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  • 13. An (X;11) translocation in a girl with Duchenne muscular dystrophy. Repository identification No. GM1695.
    Greenstein RM, Reardon MP, Chan TS, Middleton AB, Mulivor RA, Greene AE, Coriell LL.
    Cytogenet Cell Genet; 1980 Sep 25; 27(4):268. PubMed ID: 7438786
    [No Abstract] [Full Text] [Related]

  • 14. 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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  • 15. 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 27; 25(2):231-6. PubMed ID: 3777020
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  • 16. 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 27; 29(6):516-22. PubMed ID: 3742857
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  • 17. [Duchenne muscular dystrophy in a female with an X-autosome translocation].
    Narazaki O, Hanai T, Ueki Y, Mitsudome A.
    Rinsho Shinkeigaku; 1985 Apr 27; 25(4):432-6. PubMed ID: 4017373
    [No Abstract] [Full Text] [Related]

  • 18. Xp21 muscular dystrophy due to X chromosome inversion.
    Baxter PS, Maltby EL, Quarrell O.
    Neurology; 1997 Jul 27; 49(1):260. PubMed ID: 9222202
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  • 19. Common sequence motifs at the rearrangement sites of a constitutional X/autosome translocation and associated deletion.
    Giacalone JP, Francke U.
    Am J Hum Genet; 1992 Apr 27; 50(4):725-41. PubMed ID: 1347968
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  • 20. 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 Apr 27; 8(6):619-23. PubMed ID: 3826553
    [Abstract] [Full Text] [Related]

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