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

96 related items for PubMed ID: 1687519

  • 1. [Uses of RFLP analysis in detecting Duchenne muscular dystrophy gene carrier].
    Chen F.
    Zhonghua Yi Xue Za Zhi; 1991 Jun; 71(6):339-41. PubMed ID: 1687519
    [No Abstract] [Full Text] [Related]

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

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N.
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 8. Diagnosis of Duchenne and Becker muscular dystrophies by DNA polymorphism.
    Akita Y, Ohno S, Goto J, Nakano I, Takatsu M, Sugita H, Suzuki K.
    Jinrui Idengaku Zasshi; 1987 Jun; 32(2):71-82. PubMed ID: 2893850
    [No Abstract] [Full Text] [Related]

  • 9. A molecular approach to genetic counseling in the X-linked muscular dystrophies.
    Harper PS, Thomas NS.
    Am J Med Genet; 1986 Dec; 25(4):687-702. PubMed ID: 2878617
    [Abstract] [Full Text] [Related]

  • 10. Germline mosaicism and Duchenne muscular dystrophy mutations.
    Bakker E, Van Broeckhoven C, Bonten EJ, van de Vooren MJ, Veenema H, Van Hul W, Van Ommen GJ, Vandenberghe A, Pearson PL.
    Nature; 1986 Dec; 329(6139):554-6. PubMed ID: 2889144
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 12. Identification of carriers of Duchenne muscular dystrophy: value of molecular analysis.
    LeRoy BS, Uhrhammer NA, Steere KJ, Boehm CD, King RA, Rich SS, Williams PP, Smith SA, de Martinville B.
    Am J Med Genet; 1988 Nov; 31(3):709-21. PubMed ID: 2906525
    [Abstract] [Full Text] [Related]

  • 13. Experience with DNA analysis in Duchenne and Becker muscular dystrophy families in NSW.
    Morgan G, Donald JA, Chen J, Serravalle S, Colley P, Denton MJ.
    Aust Paediatr J; 1988 Nov; 24 Suppl 1():98-9. PubMed ID: 3202741
    [Abstract] [Full Text] [Related]

  • 14. [New aspects of carrier diagnosis and human genetic counseling in Duchenne and Becker muscular dystrophy].
    Spiegler AW, Huppert P, Werner W, Metzke H, Strobel U, Köhler K, Gerhardt R, Kaufmann J, Herrmann FH.
    Z Arztl Fortbild (Jena); 1988 Nov; 82(22):1139-42. PubMed ID: 3247797
    [No Abstract] [Full Text] [Related]

  • 15. Update: Duchenne muscular dystrophy.
    Fenichel GM, Robison JD.
    Compr Ther; 1988 Jul; 14(7):29-32. PubMed ID: 3060302
    [No Abstract] [Full Text] [Related]

  • 16. DMD carrier detection and prenatal diagnosis via recombinant DNA methods.
    Caskey CT, Ward P, Hejtmancik F.
    Adv Neurol; 1988 Jul; 48():83-91. PubMed ID: 2891260
    [No Abstract] [Full Text] [Related]

  • 17. Dystrophin immunocytochemistry in muscle culture: detection of a carrier of Duchenne muscular dystrophy.
    Miranda AF, Francke U, Bonilla E, Martucci G, Schmidt B, Salviati G, Rubin M.
    Am J Med Genet; 1989 Feb; 32(2):268-73. PubMed ID: 2648829
    [Abstract] [Full Text] [Related]

  • 18. Molecular biology of Duchenne and Becker's muscular dystrophy: clinical applications.
    Gutmann DH, Fischbeck KH.
    Ann Neurol; 1989 Aug; 26(2):189-94. PubMed ID: 2673003
    [Abstract] [Full Text] [Related]

  • 19. A grandpaternally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome.
    Wood S, Shukin RJ, McGillivray BC, Ray PN, Worton RG.
    Am J Med Genet; 1988 Feb; 29(2):419-23. PubMed ID: 2895584
    [Abstract] [Full Text] [Related]

  • 20. [A manifested carrier of late onset Duchenne type muscular dystrophy].
    Wakata N, Uchida A, Kinoshita M.
    Rinsho Shinkeigaku; 1987 May; 27(5):630-3. PubMed ID: 3621760
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.