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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

254 related items for PubMed ID: 1476571

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  • 23. Dystrophin analysis using a panel of anti-dystrophin antibodies in Duchenne and Becker muscular dystrophy.
    Muntoni F, Mateddu A, Cianchetti C, Marrosu MG, Clerk A, Cau M, Congiu R, Cao A, Melis MA.
    J Neurol Neurosurg Psychiatry; 1993 Jan; 56(1):26-31. PubMed ID: 8429320
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  • 24. A homologue of dystrophin is expressed at the blood vessel membrane of DMD and BMD patients: immunological evidence.
    Augier N, Boucraut J, Léger J, Anoal M, Nicholson LV, Voelkel MA, Léger JJ, Pellissier JF.
    J Neurol Sci; 1992 Feb; 107(2):233-8. PubMed ID: 1564523
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  • 26. Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis.
    Gold R, Kress W, Meurers B, Meng G, Reichmann H, Müller CR.
    Muscle Nerve; 1992 Feb; 15(2):214-8. PubMed ID: 1549142
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  • 28. Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin.
    Bulman DE, Murphy EG, Zubrzycka-Gaarn EE, Worton RG, Ray PN.
    Am J Hum Genet; 1991 Feb; 48(2):295-304. PubMed ID: 1990838
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  • 30. Deletion screening of the Duchenne/Becker muscular dystrophy gene in Croatian population.
    Sertić J, Barisić N, Sostarko M, Brzović Z, Stavljenić-Rukavina A.
    Coll Antropol; 1997 Jun; 21(1):151-6. PubMed ID: 9225508
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  • 34. [Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].
    Grinchuk OV, Khidiiatova IM, Kiselev AV, Magzhanov RV, Khusnutdinova EK.
    Genetika; 1999 Apr; 35(4):551-5. PubMed ID: 10420280
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  • 38. Detection of 98% of DMD/BMD gene deletions by polymerase chain reaction.
    Beggs AH, Koenig M, Boyce FM, Kunkel LM.
    Hum Genet; 1990 Nov; 86(1):45-8. PubMed ID: 2253937
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