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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

149 related items for PubMed ID: 3995787

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  • 3. Use of serum creatine kinase, pyruvate kinase, and genetic linkage for carrier detection in Duchenne and Becker dystrophy.
    Hyser CL, Griggs RC, Mendell JR, Polakowska R, Quirk S, Brooke MH, Fenichel GM, Doherty RA.
    Neurology; 1987 Jan; 37(1):4-10. PubMed ID: 2879259
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  • 4. 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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  • 9. The contribution of assays for lymphocyte capping and creatine kinase to detection of the Becker-type dystrophy trait.
    Goldsmith BM, Gruemer HD, Hawley RJ, Pickard NA, Verrill HL, Nance WE, Miller G, Crawford RG.
    Clin Chem; 1980 May; 26(6):754-9. PubMed ID: 7371153
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  • 12. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC, Gedeon AK, Haan EA, Sheffield LJ, White SJ, Bates LJ, Robertson EF, Sutherland GR.
    Aust Paediatr J; 1988 May; 24 Suppl 1():92-7. PubMed ID: 3202740
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  • 13. [Carrier diagnosis and prenatal prognosis using DNA analysis in X-chromosome-linked Duchenne and Becker muscular dystrophy].
    Moser H, Liechti-Gallati S, Braga S, Hirsiger H.
    Schweiz Med Wochenschr; 1987 Dec 19; 117(51):2061-73. PubMed ID: 3433090
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  • 19. Benign muscular dystrophy: risk calculation in families with consanguinity.
    Wolff G, Müller CR, Grimm T.
    J Med Genet; 1989 May 19; 26(5):299-304. PubMed ID: 2732990
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