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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

219 related items for PubMed ID: 2668030

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  • 2. Unraveling the mysteries of Duchenne and Becker muscular dystrophy.
    Hyser CL.
    Mol Chem Neuropathol; 1989 Feb; 10(1):15-20. PubMed ID: 2660836
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  • 3. Effect of dystrophin gene deletions on mRNA levels and processing in Duchenne and Becker muscular dystrophies.
    Chelly J, Gilgenkrantz H, Lambert M, Hamard G, Chafey P, Récan D, Katz P, de la Chapelle A, Koenig M, Ginjaar IB.
    Cell; 1990 Dec 21; 63(6):1239-48. PubMed ID: 2261642
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  • 10. Characterization of pathological dystrophin transcripts from the lymphocytes of a muscular dystrophy carrier.
    Schloesser M, Slomski R, Wagner M, Reiss J, Berg LP, Kakkar VV, Cooper DN.
    Mol Biol Med; 1990 Dec 21; 7(6):519-23. PubMed ID: 1706453
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  • 11. An informative polymorphism detectable by polymerase chain reaction at the 3' end of the dystrophin gene.
    Oudet C, Heilig R, Mandel JL.
    Hum Genet; 1990 Feb 21; 84(3):283-5. PubMed ID: 1968037
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  • 14. [Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA].
    Saito K, Tanaka A, Harada T, Ikeya K, Fukuyama Y, Arahata K, Sugita H, Osawa M, Shishikura K, Suzuki H.
    No To Hattatsu; 1989 Jul 21; 21(4):361-8. PubMed ID: 2675944
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  • 16. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
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  • 17. Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.
    Norman A, Thomas N, Coakley J, Harper P.
    Lancet; 1989 Mar 04; 1(8636):466-8. PubMed ID: 2563842
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