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Journal Abstract Search

196 related items for PubMed ID: 9733048

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  • 2. [CTG-repeat analysis of myotonin protein kinase gene in Bashkortostan patients with myotonic dystrophy].
    Khidiiatova IM, Fatkhlislamova RI, magzhanov RV, Popova SN, Slominskiĭ PA, Limborskaia SA, Khusnutdinova EK.
    Zh Nevrol Psikhiatr Im S S Korsakova; 2002; 102(3):54-8. PubMed ID: 11957350
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  • 5. CTG triplet repeat expansion in a laryngeal carcinoma from a patient with myotonic dystrophy.
    Osanai R, Kinoshita M, Hirose K, Homma T, Kawabata I.
    Muscle Nerve; 2000 May; 23(5):804-6. PubMed ID: 10797405
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  • 6. Eight years' experience of direct molecular testing for myotonic dystrophy in Wales.
    Fokstuen S, Myring J, Meredith L, Ravine D, Harper PS.
    J Med Genet; 2001 Dec; 38(12):E42. PubMed ID: 11748308
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  • 8. CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand.
    Theerasasawat S, Papsing C, Pulkes T.
    J Clin Neurosci; 2010 Dec; 17(12):1520-2. PubMed ID: 20801043
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  • 12. [Disease picture of myotonic muscular dystrophy in patients with large CTG triplet expansion].
    Spranger M, Janssen B, Rating D, Spranger S.
    Nervenarzt; 1999 Feb; 70(2):131-5. PubMed ID: 10098148
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  • 13. CTG expansion & haplotype analysis in DM1 gene in healthy Iranian population.
    Shojasaffar B, Moradin N, Kahrizi K, Cobo AM, Najmabadi H.
    Can J Neurol Sci; 2008 May; 35(2):216-9. PubMed ID: 18574937
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  • 14. Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levels.
    Eriksson M, Ansved T, Edström L, Anvret M, Carey N.
    Hum Mol Genet; 1999 Jun; 8(6):1053-60. PubMed ID: 10332037
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  • 16. De novo myotonic dystrophy mutation in a Nigerian kindred.
    Krahe R, Eckhart M, Ogunniyi AO, Osuntokun BO, Siciliano MJ, Ashizawa T.
    Am J Hum Genet; 1995 May; 56(5):1067-74. PubMed ID: 7726160
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  • 17. Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)?
    Abbruzzese C, Krahe R, Liguori M, Tessarolo D, Siciliano MJ, Ashizawa T, Giacanelli M.
    J Neurol; 1996 Oct; 243(10):715-21. PubMed ID: 8923304
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  • 18. Surgical repair for atrial septal defect associated with myotonic dystrophy.
    Ogawa T, Saga T, Nakamoto S.
    Circ J; 2007 Aug; 71(8):1321-2. PubMed ID: 17652903
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  • 19. Paternal transmission of the congenital form of myotonic dystrophy type 1: a new case and review of the literature.
    Zeesman S, Carson N, Whelan DT.
    Am J Med Genet; 2002 Jan 22; 107(3):222-6. PubMed ID: 11807903
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