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PUBMED FOR HANDHELDS

Journal Abstract Search


188 related items for PubMed ID: 6490012

  • 1. X-linked Duchenne muscular dystrophy in an unusual family with manifesting carriers.
    Kaladhar Reddy B, Anandavalli TE, Reddi OS.
    Hum Genet; 1984; 67(4):460-2. PubMed ID: 6490012
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  • 2. Duchenne type muscular dystrophy and consanguinity: difficulties in pedigree analysis.
    Aymé S, Pelissier JF, Garnier JM, Mattei JF, Giraud F.
    J Med Genet; 1979 Oct; 16(5):393-5. PubMed ID: 513086
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  • 3. A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales.
    Norman A, Harper P.
    Clin Genet; 1989 Jul; 36(1):31-7. PubMed ID: 2766561
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  • 6. Use of normal daughters' and sisters' creatine kinase levels in estimating heterozygosity in Duchenne muscular dystrophy.
    Emery AE, Holloway S.
    Hum Hered; 1977 Jul; 27(2):118-26. PubMed ID: 863458
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  • 8. Genetic counseling in Becker type X-linked muscular dystrophy. II: Practical considerations.
    Grimm T.
    Am J Med Genet; 1984 Aug; 18(4):719-23. PubMed ID: 6486170
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  • 10. Detection of carriers of X-linked gene for Duchenne muscular dystrophy by levels of creatine kinase and pyruvate kinase.
    Falcão-Conceição DN, Gonçalves-Pimentel MM, Baptista ML, Ubatuba S.
    J Neurol Sci; 1983 Dec; 62(1-3):171-80. PubMed ID: 6668472
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  • 11. Carrier detection of Duchenne muscular dystrophy through analysis of DNA from deciduous teeth of a dead affected child.
    Restagno G, Ferrone M, Doriguzzi C, Palmucci L, Mongini T, Carbonara A.
    Prenat Diagn; 1995 Jul; 15(7):672-4. PubMed ID: 8532630
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  • 12. X linked muscular dystrophy with contractures.
    Johnston AW, McKay E.
    J Med Genet; 1986 Dec; 23(6):591-5. PubMed ID: 3806639
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  • 13. Monozygotic female twin carriers discordant for the clinical manifestations of Duchenne muscular dystrophy.
    Chutkow JG, Hyser CL, Edwards JA, Heffner RR, Czyrny JJ.
    Neurology; 1987 Jul; 37(7):1147-51. PubMed ID: 2885783
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  • 15. Female carriers of Duchenne muscular dystrophy: a dilemma.
    Isaacs H, Badenhorst M.
    Clin Genet; 1987 May; 31(5):288-96. PubMed ID: 3608214
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  • 16. The manifesting carrier in Duchenne muscular dystrophy.
    Moser H, Emery AE.
    Clin Genet; 1974 May; 5(4):271-84. PubMed ID: 4854942
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  • 17. Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.
    Passos-Bueno MR, Vainzof M, Pavanello Rde C, Pavanello-Filho I, Lima MA, Zatz M.
    J Neurol Sci; 1991 May; 103(1):65-75. PubMed ID: 1865235
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  • 18. Reflections on muscular dystrophy in a Sudanese kindred.
    Salih MA, Roberts DF, Omer MI, Karrar O, Bayoumi RA.
    Clin Genet; 1983 Apr; 23(4):325-8. PubMed ID: 6851225
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