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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

139 related items for PubMed ID: 2591962

  • 21.
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  • 22. Physical mapping and cloning of the proximal segment of the myotonic dystrophy gene region.
    Shutler G, Korneluk RG, Tsilfidis C, Mahadevan M, Bailly J, Smeets H, Jansen G, Wieringa B, Lohman F, Aslanidis C.
    Genomics; 1992 Jul; 13(3):518-25. PubMed ID: 1639380
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  • 24. Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.
    MacKenzie AE, MacLeod HL, Hunter AG, Korneluk RG.
    Am J Hum Genet; 1989 Jan; 44(1):140-7. PubMed ID: 2562820
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  • 28. A reordering of human chromosome 19 long-arm DNA markers and identification of markers flanking the myotonic dystrophy locus.
    Korneluk RG, MacKenzie AE, Nakamura Y, Dubé I, Jacob P, Hunter AG.
    Genomics; 1989 Oct; 5(3):596-604. PubMed ID: 2613241
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  • 32. Characterization of a YAC and cosmid contig containing markers tightly linked to the myotonic dystrophy locus on chromosome 19.
    Buxton J, Shelbourne P, Davies J, Jones C, Perryman MB, Ashizawa T, Butler R, Brook D, Shaw D, de Jong P.
    Genomics; 1992 Jul; 13(3):526-31. PubMed ID: 1639381
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  • 33. The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.
    MacKenzie AE, Korneluk RG, Zorzato F, Fujii J, Phillips M, Iles D, Wieringa B, Leblond S, Bailly J, Willard HF.
    Am J Hum Genet; 1990 Jun; 46(6):1082-9. PubMed ID: 1971150
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  • 34. A new probe for the diagnosis of myotonic muscular dystrophy.
    Bartlett RJ, Pericak-Vance MA, Yamaoka L, Gilbert J, Herbstreith M, Hung WY, Lee JE, Mohandas T, Bruns G, Laberge C.
    Science; 1987 Mar 27; 235(4796):1648-50. PubMed ID: 3029876
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  • 38. [Myotonic dystrophy of Steinert].
    Junien C.
    J Genet Hum; 1989 Jan 27; 37(1):51-4. PubMed ID: 2565953
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