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Journal Abstract Search

310 related items for PubMed ID: 8629100

  • 1. Detection of DMD gene deletions in Thai children patients.
    Kamolsilp M, Paditaporn R, Noonai A, Wasant P.
    Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():172-4. PubMed ID: 8629100
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  • 4. Multiplex PCR to detect the dystrophin gene deletion in Thai patients.
    Mutirangura A, Jongpiputvanich S, Norapucsunton T, Theamboonlers A, Srivuthana S, Promchainant C, Tumwasorn S, Sueblinvong T.
    J Med Assoc Thai; 1995 Sep; 78(9):460-5. PubMed ID: 7561572
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  • 5. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T, Matsuo M, Nakamura H, Fujiwara Y.
    Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
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  • 6. Pattern of deletions of the dystrophin gene in Mexican Duchenne/Becker muscular dystrophy patients: the use of new designed primers for the analysis of the major deletion "hot spot" region.
    Coral-Vazquez R, Arenas D, Cisneros B, Peñaloza L, Salamanca F, Kofman S, Mercado R, Montañez C.
    Am J Med Genet; 1997 Jun 13; 70(3):240-6. PubMed ID: 9188659
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  • 7. 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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  • 8. 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 15; 21(1):151-6. PubMed ID: 9225508
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  • 10. Are there ethnic differences in deletions in the dystrophin gene?
    Banerjee M, Verma IC.
    Am J Med Genet; 1997 Jan 20; 68(2):152-7. PubMed ID: 9028449
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  • 17. Molecular genetic and immunological analysis of dystrophin of a young patient with X-linked muscular dystrophy.
    Ikeya K, Saito K, Hayashi K, Tanaka H, Hagiwara Y, Yoshida M, Yamauchi A, Fukuyama Y, Ishiguro T, Eguchi C.
    Am J Med Genet; 1992 Jun 01; 43(3):580-7. PubMed ID: 1605252
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  • 18. Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin.
    Le Thiet Thanh, Nguyen Thi Man, Hori S, Sewry CA, Dubowitz V, Morris GE.
    Am J Med Genet; 1995 Aug 28; 58(2):177-86. PubMed ID: 8533812
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  • 19. Amplification of selected exons by polymerase chain reaction enables determination of the translational reading frame of dystrophin mRNA resulting from deletion mutations.
    Kitoh Y, Matsuo M, Nishio H, Nakamura H.
    Kobe J Med Sci; 1994 Apr 28; 40(2):39-48. PubMed ID: 7823533
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