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Journal Abstract Search

207 related items for PubMed ID: 8105117

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  • 5. [Microsatellite analysis of Duchenne muscular dystrophy].
    Fujishita S, Shibuya N.
    Nihon Rinsho; 1997 Dec; 55(12):3131-6. PubMed ID: 9436423
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  • 6. Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
    Fujishita S, Shibuya N, Niikawa N, Nagataki S.
    Jinrui Idengaku Zasshi; 1991 Dec; 36(4):317-24. PubMed ID: 1811098
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  • 10. [Analysis of deletions in the dystrophin gene in patients with Duchenne muscular dystrophy in the Bashkir Republic].
    Grinchuk OV, Khidiiatova IM, Kiselev AV, Magzhanov RV, Khusnutdinova EK.
    Genetika; 1999 Apr; 35(4):551-5. PubMed ID: 10420280
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  • 11. Direct method for prenatal diagnosis and carrier detection in Duchenne/Becker muscular dystrophy using the entire dystrophin cDNA.
    Darras BT, Koenig M, Kunkel LM, Francke U.
    Am J Med Genet; 1988 Mar; 29(3):713-26. PubMed ID: 2897793
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  • 12. Prenatal diagnosis of Duchenne muscular dystrophy by polymerase chain reaction analysis.
    Katayama S, Takeshita N, Yano T, Katagiri Y, Shirosita Y, Kubo H, Hirakawa S, Ubagai T.
    Fetal Diagn Ther; 1994 Mar; 9(6):379-84. PubMed ID: 7880434
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  • 13. DNA polymorphisms and deletion analysis of the Duchenne-Becker muscular dystrophy gene in the Chinese.
    Soong BW, Tsai TF, Su CH, Kao KP, Hsiao KJ, Su TS.
    Am J Med Genet; 1991 Mar 15; 38(4):593-600. PubMed ID: 1676564
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  • 19. Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR.
    Gökgöz N, Kuseyri F, Topaloğlu H, Yüksel-Apak M, Kirdar B.
    Clin Genet; 1993 May 15; 43(5):261-6. PubMed ID: 8104108
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  • 20. Allele frequencies of intragenic, and 5' and 3' markers of the dystrophin gene in Japanese families afflicted with Duchenne or Becker muscular dystrophy.
    Tsukamoto H, Inui K, Fukushima H, Okada S.
    Jpn J Hum Genet; 1996 Dec 15; 41(4):391-7. PubMed ID: 9088109
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