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Journal Abstract Search


150 related items for PubMed ID: 2889145

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  • 8. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
    Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM.
    Nature; ; 323(6089):646-50. PubMed ID: 3773991
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  • 10. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 15. Update on the molecular genetics of Duchenne muscular dystrophy.
    Siddique T, Bartlett R, Pericak-Vance M, Yamaoka L, Koh J, Chen J, Hung WY, Kandt R, Roses AD.
    Aust Paediatr J; 1988 Aug; 24 Suppl 1():9-14. PubMed ID: 3060079
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  • 16. Brother/sister pairs affected with early-onset, progressive muscular dystrophy: molecular studies reveal etiologic heterogeneity.
    Francke U, Darras BT, Hersh JH, Berg BO, Miller RG.
    Am J Hum Genet; 1989 Jul; 45(1):63-72. PubMed ID: 2568091
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  • 18. Pulsed-field gel electrophoresis of the D4F104S1 locus reveals the size and the parental origin of the facioscapulohumeral muscular dystrophy (FSHD)-associated deletions.
    Wijmenga C, van Deutekom JC, Hewitt JE, Padberg GW, van Ommen GJ, Hofker MH, Frants RR.
    Genomics; 1994 Jan 01; 19(1):21-6. PubMed ID: 7910579
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  • 19. Pathogenic and nonpathogenic deletions in two families with Duchenne muscular dystrophy.
    Hart KA, Abbs S, Bobrow M.
    Am J Med Genet; 1989 May 01; 33(1):142-5. PubMed ID: 2750784
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