These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

176 related items for PubMed ID: 9436423

  • 1. [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]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3. [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 Dec; 30(2):193-9; quiz 200. PubMed ID: 8756246
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. 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 Dec; 5(2):183-5. PubMed ID: 7917130
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. 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; 21(3):567-70. PubMed ID: 7959733
    [Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. Prenatal diagnosis of Duchenne/Becker muscular dystrophy by short tandem repeat segregation analysis in Argentine families.
    Giliberto F, Ferreiro V, Massot F, Ferrer M, Francipane L, Szijan I.
    Muscle Nerve; 2011 Apr; 43(4):510-7. PubMed ID: 21305566
    [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; 36(4):317-24. PubMed ID: 1811098
    [Abstract] [Full Text] [Related]

  • 16. Eight novel microsatellite markers in the 3' region of the dystrophin gene useful for diagnosis of Duchenne muscular dystrophy.
    Matsumoto T, Niikawa N.
    Prenat Diagn; 2004 Dec 15; 24(12):1014-5. PubMed ID: 15612059
    [No Abstract] [Full Text] [Related]

  • 17. Use of dystrophin genomic and cDNA probes for solving difficulties in carrier detection and prenatal diagnosis of Duchenne muscular dystrophy.
    Shomrat R, Driks N, Legum C, Shiloh Y.
    Am J Med Genet; 1992 Feb 01; 42(3):281-7. PubMed ID: 1536162
    [Abstract] [Full Text] [Related]

  • 18. [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]

  • 19. Prenatal diagnosis of Duchenne muscular dystrophy in the Japanese population by fluorescent CA repeat polymorphisms analysis.
    Shiroshita Y, Katayama S.
    J Obstet Gynaecol Res; 1997 Oct 01; 23(5):453-61. PubMed ID: 9392912
    [Abstract] [Full Text] [Related]

  • 20. Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in Russia.
    Baranov VS, Gorbunova VN, Malysheva OV, Artemyeva OV, Kascheeva TK, Evgrafov OV, Polyakov AV, Lebedev VM, Kuznetzova TV, Shlykova SN.
    Prenat Diagn; 1993 May 01; 13(5):323-33. PubMed ID: 8101987
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.