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Journal Abstract Search

149 related items for PubMed ID: 1681950

  • 1. Deletion analysis of Duchenne muscular dystrophy using cDNA probes and multiplex PCR.
    Radosavljević D, Todorović D, Crkvenjakov R.
    Neurol Croat; 1991; 40(3):157-64. PubMed ID: 1681950
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  • 6. Carrier detection by DNA analysis in Duchenne muscular dystrophy families.
    Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Ozdemir C, Kuseyri F, Apak MY, Tolun A.
    Turk J Pediatr; 1992; 34(2):79-92. PubMed ID: 1440954
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  • 9. Molecular deletion patterns in Duchenne muscular dystrophy patients.
    Lucotte G, David F, Levy C.
    Ann Genet; 1989; 32(4):214-9. PubMed ID: 2610487
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  • 12. 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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  • 14. 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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  • 16. [Rapid screening of the Duchenne muscular dystrophy gene deletion by two multiplex PCR].
    Ma S.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Feb; 15(1):74-8. PubMed ID: 8324844
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  • 17. Deletion analysis of the dystrophin gene in Duchenne and Becker muscular dystrophy patients: use in carrier diagnosis.
    Kumari D, Mital A, Gupta M, Goyle S.
    Neurol India; 2003 Jun; 51(2):223-6. PubMed ID: 14571009
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  • 20. [Detection of deletions by the amplification of exons (multiplex PCR) in Duchenne muscular dystrophy].
    Claustres M, Kjellberg P, Desgeorges M, Bellet H, Sarda P, Bonnet H, Boileau C.
    J Genet Hum; 1989 Sep; 37(3):251-7. PubMed ID: 2625628
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