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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

265 related items for PubMed ID: 7849703

  • 61.
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  • 62. Genetic linkage map of facioscapulohumeral muscular dystrophy and five polymorphic loci on chromosome 4q35-qter.
    Wijmenga C, Sandkuijl LA, Moerer P, van der Boorn N, Bodrug SE, Ray PN, Brouwer OF, Murray JC, van Ommen GJ, Padberg GW.
    Am J Hum Genet; 1992 Aug; 51(2):411-5. PubMed ID: 1642239
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  • 63. A novel tandem repeat sequence located on human chromosome 4p: isolation and characterization.
    Kogi M, Fukushige S, Lefevre C, Hadano S, Ikeda JE.
    Genomics; 1997 Jun 01; 42(2):278-83. PubMed ID: 9192848
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  • 67. High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint.
    Grewal PK, Bolland DJ, Todd LC, Hewitt JE.
    Mamm Genome; 1998 Aug 01; 9(8):603-7. PubMed ID: 9680377
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  • 68. Efforts toward understanding the molecular basis of facioscapulohumeral muscular dystrophy.
    Altherr MR, Bengtsson U, Markovich RP, Winokur ST.
    Muscle Nerve Suppl; 1995 Aug 01; (2):S32-8. PubMed ID: 23573584
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  • 69. Chromosome 4q35 haplotypes and DNA rearrangements segregating in affected subjects of 19 Italian families with facioscapulohumeral muscular dystrophy (FSHD).
    Cacurri S, Deidda G, Piazzo N, Novelletto A, La Cesa I, Servidei S, Galluzzi G, Wijmenga C, Frants RR, Felicetti L.
    Hum Genet; 1994 Oct 01; 94(4):367-74. PubMed ID: 7927331
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  • 70.
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  • 72. Molecular analysis of a novel subtelomeric repeat with polymorphic chromosomal distribution.
    Martin-Gallardo A, Lamerdin J, Sopapan P, Friedman C, Fertitta AL, Garcia E, Carrano A, Negorev D, Macina RA, Trask BJ.
    Cytogenet Cell Genet; 1995 Oct 01; 71(3):289-95. PubMed ID: 7587396
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  • 73.
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  • 75. Structure and variability of human chromosome ends.
    de Lange T, Shiue L, Myers RM, Cox DR, Naylor SL, Killery AM, Varmus HE.
    Mol Cell Biol; 1990 Feb 01; 10(2):518-27. PubMed ID: 2300052
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  • 76.
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  • 77. Comparative sequence analysis of primate subtelomeres originating from a chromosome fission event.
    Rudd MK, Endicott RM, Friedman C, Walker M, Young JM, Osoegawa K, NISC Comparative Sequencing Program, de Jong PJ, Green ED, Trask BJ.
    Genome Res; 2009 Jan 01; 19(1):33-41. PubMed ID: 18952852
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  • 78. Facioscapulohumeral muscular dystrophy: the impact of genetic research.
    Brouwer OF, Wijmenga C, Frants RR, Padberg GW.
    Clin Neurol Neurosurg; 1993 Mar 01; 95(1):9-21. PubMed ID: 8095870
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  • 79. Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus.
    de Martinville B, Kunkel LM, Bruns G, Morlé F, Koenig M, Mandel JL, Horwich A, Latt SA, Gusella JF, Housman D.
    Am J Hum Genet; 1985 Mar 01; 37(2):235-49. PubMed ID: 2984924
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  • 80. De novo facioscapulohumeral muscular dystrophy: frequent somatic mosaicism, sex-dependent phenotype, and the role of mitotic transchromosomal repeat interaction between chromosomes 4 and 10.
    van der Maarel SM, Deidda G, Lemmers RJ, van Overveld PG, van der Wielen M, Hewitt JE, Sandkuijl L, Bakker B, van Ommen GJ, Padberg GW, Frants RR.
    Am J Hum Genet; 2000 Jan 01; 66(1):26-35. PubMed ID: 10631134
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