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PUBMED FOR HANDHELDS

Journal Abstract Search

278 related items for PubMed ID: 7334502

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22. Xp21/A translocation: a rarely considered genetic cause for manifesting carriers of duchenne muscular dystrophy.
    Trippe H, Wieczorek S, Kötting J, Kress W, Schara U.
    Neuropediatrics; 2014 Oct; 45(5):333-5. PubMed ID: 25046452
    [Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
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  • 24. Inherited deletion of subband Xp21.13 in a male with Duchenne muscular dystrophy.
    Werner W, Spiegler AW.
    J Med Genet; 1988 Jun; 25(6):377-82. PubMed ID: 3294410
    [Abstract] [Full Text] [Related]

  • 25. Sequence analysis of the breakpoint regions of an X;5 translocation in a female with Duchenne muscular dystrophy.
    van Bakel I, Holt S, Craig I, Boyd Y.
    Am J Hum Genet; 1995 Aug; 57(2):329-36. PubMed ID: 7668258
    [Abstract] [Full Text] [Related]

  • 26. Long-range genomic map of the Duchenne muscular dystrophy (DMD) gene: isolation and use of J66 (DXS268), a distal intragenic marker.
    van Ommen GJ, Bertelson C, Ginjaar HB, den Dunnen JT, Bakker E, Chelly J, Matton M, van Essen AJ, Bartley J, Kunkel LM.
    Genomics; 1987 Dec; 1(4):329-36. PubMed ID: 2896627
    [Abstract] [Full Text] [Related]

  • 27. DNA studies in a family with Duchenne muscular dystrophy and a deletion at Xp21.
    Greenberg CR, Hamerton JL, Nigli M, Wrogemann K.
    Am J Hum Genet; 1987 Aug; 41(2):128-37. PubMed ID: 3475976
    [Abstract] [Full Text] [Related]

  • 28. X;autosome translocations in females with Duchenne or Becker muscular dystrophy.
    Dubowitz V.
    Nature; 1987 Aug; 322(6076):291-2. PubMed ID: 3461282
    [No Abstract] [Full Text] [Related]

  • 29. In utero fetal muscle biopsy for the diagnosis of Duchenne muscular dystrophy in a female fetus "suddenly at risk".
    Evans MI, Farrell SA, Greb A, Ray P, Johnson MP, Hoffman EP.
    Am J Med Genet; 1993 May 15; 46(3):309-12. PubMed ID: 8488877
    [Abstract] [Full Text] [Related]

  • 30. Molecular heterogeneity of translocations associated with muscular dystrophy.
    Boyd Y, Munro E, Ray P, Worton R, Monaco T, Kunkel L, Craig I.
    Clin Genet; 1987 Apr 15; 31(4):265-72. PubMed ID: 3594934
    [Abstract] [Full Text] [Related]

  • 31. A cDNA clone from the Duchenne/Becker muscular dystrophy gene.
    Burghes AH, Logan C, Hu X, Belfall B, Worton RG, Ray PN.
    Nature; 1987 Apr 15; 328(6129):434-7. PubMed ID: 3614347
    [Abstract] [Full Text] [Related]

  • 32. 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 Apr 15; 27(4):268. PubMed ID: 7438786
    [No Abstract] [Full Text] [Related]

  • 33. 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; 1980 Apr 15; 316(6031):842-5. PubMed ID: 2993910
    [Abstract] [Full Text] [Related]

  • 34. [Duchenne muscular dystrophy (DMD) in a female with an X-autosome translocation].
    Uchida T, Ogata H, Shirai Z, Mitsudome A.
    No To Hattatsu; 1988 Jan 15; 20(1):28-32. PubMed ID: 3279979
    [No Abstract] [Full Text] [Related]

  • 35. Duchenne muscular dystrophy due to familial Xp21 deletion detectable by DNA analysis and flow cytometry.
    Wilcox DE, Cooke A, Colgan J, Boyd E, Aitken DA, Sinclair L, Glasgow L, Stephenson JB, Ferguson-Smith MA.
    Hum Genet; 1986 Jun 15; 73(2):175-80. PubMed ID: 3721503
    [Abstract] [Full Text] [Related]

  • 36. Duchenne muscular dystrophy involving translocation of the dmd gene next to ribosomal RNA genes.
    Worton RG, Duff C, Sylvester JE, Schmickel RD, Willard HF.
    Science; 1984 Jun 29; 224(4656):1447-9. PubMed ID: 6729462
    [Abstract] [Full Text] [Related]

  • 37. [Duchenne muscular dystrophy in a female with an X-autosome translocation].
    Narazaki O, Hanai T, Ueki Y, Mitsudome A.
    Rinsho Shinkeigaku; 1985 Apr 29; 25(4):432-6. PubMed ID: 4017373
    [No Abstract] [Full Text] [Related]

  • 38. 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
    [Abstract] [Full Text] [Related]

  • 39. Isolation of a conserved sequence deleted in Duchenne muscular dystrophy patients.
    Smith TJ, Wilson L, Kenwrick SJ, Forrest SM, Speer A, Coutelle C, Davies KE.
    Nucleic Acids Res; 1987 Mar 11; 15(5):2167-74. PubMed ID: 3562224
    [Abstract] [Full Text] [Related]

  • 40. The problem of Duchenne muscular dystrophy.
    Worton RG, Ray PN, Bodrug S, Burghes AH, Hu X, Thompson MW.
    Philos Trans R Soc Lond B Biol Sci; 1988 Jun 15; 319(1194):275-84. PubMed ID: 2900521
    [Abstract] [Full Text] [Related]

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