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

170 related items for PubMed ID: 2643315

  • 1. Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.
    Ward PA, Hejtmancik JF, Witkowski JA, Baumbach LL, Gunnell S, Speer J, Hawley P, Tantravahi U, Caskey CT.
    Am J Hum Genet; 1989 Feb; 44(2):270-81. PubMed ID: 2643315
    [Abstract] [Full Text] [Related]

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

  • 3. Dystrophin analysis in duchenne muscular dystrophy: use in fetal diagnosis and in genetic counseling.
    Bieber FR, Hoffman EP, Amos JA.
    Am J Hum Genet; 1989 Sep; 45(3):362-7. PubMed ID: 2672800
    [Abstract] [Full Text] [Related]

  • 4. Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA.
    Upadhyaya M, Smith RA, Thomas NS, Norman AM, Harper PS.
    Clin Genet; 1990 Jun; 37(6):456-62. PubMed ID: 2200624
    [Abstract] [Full Text] [Related]

  • 5. Duchenne and Becker muscular dystrophies: genetics, prenatal diagnosis, and future prospects.
    Bieber FR, Hoffman EP.
    Clin Perinatol; 1990 Dec; 17(4):845-65. PubMed ID: 2286031
    [Abstract] [Full Text] [Related]

  • 6. Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.
    Norman AM, Upadhyaya M, Thomas NS, Roberts K, Harper PS.
    J Med Genet; 1989 Sep; 26(9):565-71. PubMed ID: 2810340
    [Abstract] [Full Text] [Related]

  • 7. [Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA].
    Saito K, Tanaka A, Harada T, Ikeya K, Fukuyama Y, Arahata K, Sugita H, Osawa M, Shishikura K, Suzuki H.
    No To Hattatsu; 1989 Jul; 21(4):361-8. PubMed ID: 2675944
    [Abstract] [Full Text] [Related]

  • 8. Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.
    Speer A, Spiegler AW, Hanke R, Grade K, Giertler U, Schieck J, Forrest S, Davies KE, Neumann R, Bollmann R.
    J Med Genet; 1989 Jan; 26(1):1-5. PubMed ID: 2918522
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 11. 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]

  • 12. Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a.
    Herrmann FH, Wulff K, Schütz M, Wehnert M.
    Eur J Pediatr; 1990 Jan; 149(4):263-5. PubMed ID: 1968008
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. 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]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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