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Journal Abstract Search

93 related items for PubMed ID: 2891257

  • 1. X-linked muscular dystrophies: studies through functional assay and DNA polymorphisms.
    Romeo G, Rocchi M, Roncuzzi L, Ferlini A, Nobile C, Rugolo M.
    Adv Neurol; 1988; 48():31-6. PubMed ID: 2891257
    [No Abstract] [Full Text] [Related]

  • 2. Molecular analysis of human muscular dystrophies.
    Davies KE, Forrest S, Smith T, Kenwrick S, Ball S, Dorkins H, Patterson M.
    Muscle Nerve; 1987; 10(3):191-9. PubMed ID: 2882417
    [Abstract] [Full Text] [Related]

  • 3. Gene mapping and the muscular dystrophies.
    Harper PS.
    Prog Clin Biol Res; 1989; 306():29-49. PubMed ID: 2567999
    [No Abstract] [Full Text] [Related]

  • 4. DMD carrier detection and prenatal diagnosis via recombinant DNA methods.
    Caskey CT, Ward P, Hejtmancik F.
    Adv Neurol; 1988; 48():83-91. PubMed ID: 2891260
    [No Abstract] [Full Text] [Related]

  • 5. [DNA diagnosis of muscular dystrophies].
    Lindlöf M, Somer H.
    Duodecim; 1988; 104(22):1787-95. PubMed ID: 2905983
    [No Abstract] [Full Text] [Related]

  • 6. Mapping the facioscapulohumeral muscular dystrophy gene is complicated by chromsome 4q35 recombination events.
    Weiffenbach B, Dubois J, Storvick D, Tawil R, Jacobsen SJ, Gilbert J, Wijmenga C, Mendell JR, Winokur S, Altherr MR.
    Nat Genet; 1993 Jun; 4(2):165-9. PubMed ID: 8102297
    [Abstract] [Full Text] [Related]

  • 7. [Genetic aspects of muscular dystrophy].
    Koizumi H, Ishiura S, Sugita H.
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):1017-22. PubMed ID: 2908389
    [No Abstract] [Full Text] [Related]

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  • 10. X;autosome translocations in females with Duchenne or Becker muscular dystrophy.
    Dubowitz V.
    Nature; 1988 Apr; 322(6076):291-2. PubMed ID: 3461282
    [No Abstract] [Full Text] [Related]

  • 11. [Diagnosis of Duchenne muscular dystrophy using DNA probes].
    Evgrafov OV, Makarov VB.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1987 Apr; 87(11):1732-6. PubMed ID: 3324590
    [No Abstract] [Full Text] [Related]

  • 12. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
    Darras BT, Koenig M, Kunkel LM, Francke U.
    Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
    [Abstract] [Full Text] [Related]

  • 13. Increased chloride efflux in fibroblasts from X-linked muscular dystrophies and clones from Duchenne carriers.
    Rugolo M, Rocchi M, Lenaz G, Romeo G.
    FEBS Lett; 1987 Feb 23; 212(2):313-6. PubMed ID: 3817163
    [Abstract] [Full Text] [Related]

  • 14. Genetic strategies for neuromuscular diseases.
    Wood DS.
    Adv Neurol; 1988 Feb 23; 48():145-51. PubMed ID: 2891253
    [No Abstract] [Full Text] [Related]

  • 15. [Use of DNA analysis in the prevention of progressive muscular dystrophies].
    Kádasi L, Ferák V, Thurzová M, Kvasnicová M.
    Bratisl Lek Listy; 1988 Nov 23; 89(11):828-34. PubMed ID: 2904832
    [No Abstract] [Full Text] [Related]

  • 16. [Molecular genetics of Duchenne's disease].
    Bolhuis PA.
    Ned Tijdschr Geneeskd; 1989 Jul 08; 133(27):1347-8. PubMed ID: 2571948
    [No Abstract] [Full Text] [Related]

  • 17. Genetic counseling in Becker type X-linked muscular dystrophy. I. Theoretical considerations.
    Grimm T.
    Am J Med Genet; 1984 Aug 08; 18(4):713-8. PubMed ID: 6486169
    [Abstract] [Full Text] [Related]

  • 18. Duchenne muscular dystrophy and idiopathic hyperCKemia in a family causing confusion in genetic counselling.
    Bushby K, Goodship J, Haggerty D, Heald A, Walls T.
    Am J Med Genet; 1996 Dec 11; 66(2):237-8. PubMed ID: 8958338
    [No Abstract] [Full Text] [Related]

  • 19. Molecular genetics of the X chromosome and X-linked diseases.
    Craig IW, Goodfellow PN.
    Lab Invest; 1986 Mar 11; 54(3):241-53. PubMed ID: 3512907
    [No Abstract] [Full Text] [Related]

  • 20. Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies.
    Scheinman SJ, Pook MA, Wooding C, Pang JT, Frymoyer PA, Thakker RV.
    J Clin Invest; 1993 Jun 11; 91(6):2351-7. PubMed ID: 8099916
    [Abstract] [Full Text] [Related]

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