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Journal Abstract Search

185 related items for PubMed ID: 8756246

  • 1. [Detection of dystrophin gene mutation carrier state].
    Bisko M, Zimowski JG, Fidziańska E, Badurska B, Fidziańska A, Hausmanowa-Petrusewicz I, Zaremba J.
    Neurol Neurochir Pol; 1996; 30(2):193-9; quiz 200. PubMed ID: 8756246
    [Abstract] [Full Text] [Related]

  • 2. [Microsatellite analysis of Duchenne muscular dystrophy].
    Fujishita S, Shibuya N.
    Nihon Rinsho; 1997 Dec; 55(12):3131-6. PubMed ID: 9436423
    [Abstract] [Full Text] [Related]

  • 3. Mutation analysis of the dystrophin gene in Southern French DMD or BMD families: from Southern blot to protein truncation test.
    Tuffery S, Chambert S, Bareil C, Sarda P, Coubes C, Echenne B, Demaille J, Claustres M.
    Hum Genet; 1998 Mar; 102(3):334-42. PubMed ID: 9544849
    [Abstract] [Full Text] [Related]

  • 4. Heteroduplex analysis of the dystrophin gene: application to point mutation and carrier detection.
    Prior TW, Papp AC, Snyder PJ, Sedra MS, Western LM, Bartolo C, Moxley RT, Mendell JR.
    Am J Med Genet; 1994 Mar 01; 50(1):68-73. PubMed ID: 8160755
    [Abstract] [Full Text] [Related]

  • 5. [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 01; 35(4):551-5. PubMed ID: 10420280
    [Abstract] [Full Text] [Related]

  • 6. [Difference of new mutation rates in dystrophin gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy].
    Kawamura J, Kato S, Ishihara T, Hiraishi Y, Kawashiro T.
    Rinsho Shinkeigaku; 1997 Mar 01; 37(3):212-7. PubMed ID: 9217419
    [Abstract] [Full Text] [Related]

  • 7. A new approach to gene diagnosis of Duchenne/Becker muscular dystrophy--amplified fragment length polymorphisms.
    Xu S, Huang S, Lo WH.
    Chin Med Sci J; 1994 Sep 01; 9(3):137-42. PubMed ID: 7865831
    [Abstract] [Full Text] [Related]

  • 8. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
    Ubagai T, Katayama S.
    Jinrui Idengaku Zasshi; 1991 Sep 01; 36(3):211-27. PubMed ID: 1684391
    [Abstract] [Full Text] [Related]

  • 9. Case of the month: germline mosaicism in carriers of Duchenne muscular dystrophy.
    Prior TW, Papp AC, Snyder PJ, Mendell JR.
    Muscle Nerve; 1992 Aug 01; 15(8):960-3. PubMed ID: 1353862
    [Abstract] [Full Text] [Related]

  • 10. [Carrier and prenatal diagnosis of Duchenne and Becker muscular dystrophy by PCR methods].
    Tsukamoto H, Inui K, Okada S.
    Nihon Rinsho; 1993 Sep 01; 51(9):2428-34. PubMed ID: 8105117
    [Abstract] [Full Text] [Related]

  • 11. [Detecting carriers of a deletion in the dystrophin gene in families with a single case of Duchenne/Becker muscular dystrophy].
    Bisko M, Zimowski JG, Hoffman-Zacharska D, Hausmanowa-Petrusewicz I, Fidziańska E, Zaremba J.
    Neurol Neurochir Pol; 1999 Sep 01; 33(6):1261-7. PubMed ID: 10791028
    [Abstract] [Full Text] [Related]

  • 12. 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 01; 29(3):713-26. PubMed ID: 2897793
    [Abstract] [Full Text] [Related]

  • 13. [Carrier detection in families affected by Duchenne/Becker muscular dystrophy].
    Pikó H, Nagy B, Balog J, Bán Z, Herczegfalvi A, Karcagi V.
    Orv Hetil; 2007 Dec 23; 148(51):2403-9. PubMed ID: 18055393
    [Abstract] [Full Text] [Related]

  • 14. Linkage disequilibria among (CA)n polymorphisms in the human dystrophin gene and their implications in carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophies.
    Chakraborty R, Zhong Y, de Andrade M, Clemens PR, Fenwick RG, Caskey CT.
    Genomics; 1994 Jun 23; 21(3):567-70. PubMed ID: 7959733
    [Abstract] [Full Text] [Related]

  • 15. 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 23; 36(4):317-24. PubMed ID: 1811098
    [Abstract] [Full Text] [Related]

  • 16. A quantitative polymerase chain reaction (PCR) assay completely discriminates between Duchenne and Becker muscular dystrophy deletion carriers and normal females.
    Pastore L, Caporaso MG, Frisso G, Orsini A, Santoro L, Sacchetti L, Salvatore F.
    Mol Cell Probes; 1996 Apr 23; 10(2):129-37. PubMed ID: 8737397
    [Abstract] [Full Text] [Related]

  • 17. Molecular diagnosis of Duchenne muscular dystrophy by use of a conformational polymorphism in the absence of DNA from an affected boy.
    Tuffery S, Moine P, Sarda P, Lefort G, Boulot P, Demaille J, Claustres M.
    Genet Couns; 1994 Apr 23; 5(2):183-5. PubMed ID: 7917130
    [Abstract] [Full Text] [Related]

  • 18. Somatic mosaicism for a deletion of the dystrophin gene in a carrier of Becker muscular dystrophy.
    Voit T, Neuen-Jacob E, Mahler V, Jauch A, Cremer M.
    Eur J Pediatr; 1992 Feb 23; 151(2):112-6. PubMed ID: 1537352
    [Abstract] [Full Text] [Related]

  • 19. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
    Baiget M, del Río E, Gallano P.
    Neurologia; 1989 Oct 23; 4(8):268-76. PubMed ID: 2576910
    [Abstract] [Full Text] [Related]

  • 20. Detection of a nonsense mutation in the dystrophin gene by multiple SSCP.
    Nigro V, Politano L, Nigro G, Romano SC, Molinari AM, Puca GA.
    Hum Mol Genet; 1992 Oct 23; 1(7):517-20. PubMed ID: 1307253
    [Abstract] [Full Text] [Related]

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