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Journal Abstract Search

306 related items for PubMed ID: 2993910

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  • 2. 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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  • 7. Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy.
    Thompson MW, Ray PN, Belfall B, Duff C, Logan C, Oss I, Worton RG.
    J Med Genet; 1986 Dec; 23(6):548-55. PubMed ID: 2879926
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  • 8. Linkage analysis of two cloned DNA sequences flanking the Duchenne muscular dystrophy locus on the short arm of the human X chromosome.
    Davies KE, Pearson PL, Harper PS, Murray JM, O'Brien T, Sarfarazi M, Williamson R.
    Nucleic Acids Res; 1983 Apr 25; 11(8):2303-12. PubMed ID: 6304647
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  • 9. 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 Apr 25; 24 Suppl 1():9-14. PubMed ID: 3060079
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  • 11. Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.
    Francke U, Harper JF, Darras BT, Cowan JM, McCabe ER, Kohlschütter A, Seltzer WK, Saito F, Goto J, Harpey JP.
    Am J Hum Genet; 1987 Mar 25; 40(3):212-27. PubMed ID: 2883886
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  • 12. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.
    Koenig M, Hoffman EP, Bertelson CJ, Monaco AP, Feener C, Kunkel LM.
    Cell; 1987 Jul 31; 50(3):509-17. PubMed ID: 3607877
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  • 14. An isolated case of Duchenne muscular dystrophy (DMD) in a female with a deletion of DMD cDNA.
    Yoshioka M, Yamamoto Y, Furuyama J.
    Clin Genet; 1990 Dec 31; 38(6):474-8. PubMed ID: 2289321
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  • 15. The problem of Duchenne muscular dystrophy.
    Worton RG, Ray PN, Bodrug S, Burghes AH, Hu X, Thompson MW.
    Philos Trans R Soc Lond B Biol Sci; 1988 Jun 15; 319(1194):275-84. PubMed ID: 2900521
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  • 17. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL.
    J Med Genet; 1986 Dec 15; 23(6):573-80. PubMed ID: 2879929
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  • 18. Direct detection of more than 50% of the Duchenne muscular dystrophy mutations by field inversion gels.
    den Dunnen JT, Bakker E, Breteler EG, Pearson PL, van Ommen GJ.
    Nature; 1986 Dec 15; 329(6140):640-2. PubMed ID: 2889148
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