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

171 related items for PubMed ID: 2672800

  • 1. 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]

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

  • 3. 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]

  • 4. Prenatal diagnosis of Duchenne muscular dystrophy by fetal muscle biopsy.
    Kuller JA, Hoffman EP, Fries MH, Golbus MS.
    Hum Genet; 1992 Dec; 90(1-2):34-40. PubMed ID: 1427785
    [Abstract] [Full Text] [Related]

  • 5. In utero fetal muscle biopsy alters diagnosis and carrier risks in Duchenne and Becker muscular dystrophy.
    Evans MI, Krivchenia EL, Johnson MP, Quintero RA, King M, Pegoraro E, Hoffman EP.
    Fetal Diagn Ther; 1995 Dec; 10(2):71-5. PubMed ID: 7794517
    [Abstract] [Full Text] [Related]

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

  • 7. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP, Pegoraro E, Scacheri P, Burns RG, Taber JW, Weiss L, Spiro A, Blattner P.
    Am J Med Genet; 1996 Jun 28; 63(4):573-80. PubMed ID: 8826437
    [Abstract] [Full Text] [Related]

  • 8. 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 28; 29(3):713-26. PubMed ID: 2897793
    [Abstract] [Full Text] [Related]

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

  • 10. 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 28; 36(4):317-24. PubMed ID: 1811098
    [Abstract] [Full Text] [Related]

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

  • 12. Dystrophin protein and RFLP analysis for fetal diagnosis and carrier confirmation of Duchenne muscular dystrophy.
    Boelter WD, Burt BA, Spector EB, Hinton DR, Pavlova Z, Fujimoto A.
    Prenat Diagn; 1990 Nov 28; 10(11):703-15. PubMed ID: 1980950
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis in a female carrying a deletion close to the Duchenne locus.
    Børresen AL, Boman H, Møller P, Berg K.
    Prenat Diagn; 1988 Jan 28; 8(1):67-72. PubMed ID: 3422736
    [Abstract] [Full Text] [Related]

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

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

  • 16. The value of deletion analysis for carrier detection in Duchenne muscular dystrophy (DMD).
    Bejjani B, Finn P, Milunsky A, Amos J.
    Clin Genet; 1991 Apr 28; 39(4):245-52. PubMed ID: 2070545
    [Abstract] [Full Text] [Related]

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

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

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. In utero fetal muscle biopsy: a precious aid for the prenatal diagnosis of Duchenne muscular dystrophy.
    Heckel S, Favre R, Flori J, Koenig M, Mandel J, Gasser B, Chaigne D.
    Fetal Diagn Ther; 1999 Apr 28; 14(3):127-32. PubMed ID: 10364661
    [Abstract] [Full Text] [Related]

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