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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

265 related items for PubMed ID: 7849703

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  • 44. The FSHD region on human chromosome 4q35 contains potential coding regions among pseudogenes and a high density of repeat elements.
    van Geel M, Heather LJ, Lyle R, Hewitt JE, Frants RR, de Jong PJ.
    Genomics; 1999 Oct 01; 61(1):55-65. PubMed ID: 10512680
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  • 47. Characterization and organization of DNA sequences adjacent to the human telomere associated repeat (TTAGGG)n.
    Weber B, Collins C, Robbins C, Magenis RE, Delaney AD, Gray JW, Hayden MR.
    Nucleic Acids Res; 1990 Jun 11; 18(11):3353-61. PubMed ID: 2356126
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  • 54. Definitive molecular diagnosis of facioscapulohumeral dystrophy.
    Orrell RW, Tawil R, Forrester J, Kissel JT, Mendell JR, Figlewicz DA.
    Neurology; 1999 Jun 10; 52(9):1822-6. PubMed ID: 10371529
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  • 57. Visualization of the terminal structure of rice chromosomes 6 and 12 with multicolor FISH to chromosomes and extended DNA fibers.
    Ohmido N, Kijima K, Ashikawa I, de Jong JH, Fukui K.
    Plant Mol Biol; 2001 Oct 10; 47(3):413-21. PubMed ID: 11587512
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  • 58. A novel minisatellite at a cloned hamster telomere.
    Shampay J, Schmitt M, Bassham S.
    Chromosoma; 1995 Oct 10; 104(1):29-38. PubMed ID: 7587592
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  • 60. Towards the finer mapping of facioscapulohumeral muscular dystrophy at 4q35: construction of a laser microdissection library.
    Upadhyaya M, Osborn M, Maynard J, Altherr M, Ikeda J, Harper PS.
    Am J Med Genet; 1995 Jun 19; 60(3):244-51. PubMed ID: 7573180
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