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Journal Abstract Search

177 related items for PubMed ID: 1977943

  • 1. [DNA diagnosis in medicine].
    Nakagome Y.
    Rinsho Byori; 1990 Sep; 38(9):1020-6. PubMed ID: 1977943
    [Abstract] [Full Text] [Related]

  • 2.
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  • 3. [Use of DNA analysis in medicine].
    Sedlácek Z, Duspivová R.
    Cas Lek Cesk; 1992 Jun 19; 131(12):357-63. PubMed ID: 1354570
    [Abstract] [Full Text] [Related]

  • 4. [The molecular diagnosis of hereditary diseases. In memoriam Dr. Eduardo Aguirre Pequeño].
    Barrera Saldaña HA, Rojas Martínez A, Rivera Pérez JA, Vázquez Alemán RM, González Garay ML.
    Gac Med Mex; 1992 Jun 19; 128(6):613-20; discussion 620-1. PubMed ID: 1344797
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  • 6. [Molecular genetics in the research and diagnosis of human pathology].
    Estivill Z, Nunes V, Gallano P.
    Med Clin (Barc); 1990 Apr 14; 94(14):541-7. PubMed ID: 1972429
    [No Abstract] [Full Text] [Related]

  • 7. Basic concepts of molecular biology as applied to pediatric and adolescent gynecology.
    Layman LC.
    Obstet Gynecol Clin North Am; 1992 Mar 14; 19(1):1-26. PubMed ID: 1350082
    [Abstract] [Full Text] [Related]

  • 8. Current status of prenatal diagnosis by DNA analysis.
    Kazazian HH.
    Birth Defects Orig Artic Ser; 1990 Mar 14; 26(3):210-6. PubMed ID: 2092848
    [Abstract] [Full Text] [Related]

  • 9. Towards a complete linkage map of the human X chromosome.
    Davies KE, Williamson R.
    Horiz Biochem Biophys; 1986 Mar 14; 8():1-50. PubMed ID: 2875929
    [Abstract] [Full Text] [Related]

  • 10. Overview of principles and current uses of DNA probes in clinical and laboratory medicine.
    Narayanan S.
    Ann Clin Lab Sci; 1992 Mar 14; 22(6):353-76. PubMed ID: 1360785
    [Abstract] [Full Text] [Related]

  • 11. [Use of DNA polymorphism in the diagnosis of human genetic diseases].
    Cebrat S.
    Postepy Hig Med Dosw; 1988 Mar 14; 42(5):461-82. PubMed ID: 2908211
    [No Abstract] [Full Text] [Related]

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  • 13. 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 14; 29(3):713-26. PubMed ID: 2897793
    [Abstract] [Full Text] [Related]

  • 14. Application of DNA probes to carrier detection and prenatal diagnosis of Duchenne (and Becker) muscular dystrophy.
    Mulley JC, Gedeon AK, Haan EA, Sheffield LJ, White SJ, Bates LJ, Robertson EF, Sutherland GR.
    Aust Paediatr J; 1988 Mar 14; 24 Suppl 1():92-7. PubMed ID: 3202740
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  • 16. [Diagnostic techniques described in the study of Duchenne/Becker muscular dystrophy].
    Montejo-Pujadas Y, Zaldívar-Vaillant T, Acevedo-López AM.
    Rev Neurol; 1988 Mar 14; 34(3):278-81. PubMed ID: 12022080
    [Abstract] [Full Text] [Related]

  • 17. Basic principles of recombinant DNA use for prenatal diagnosis.
    Goldberg JD.
    Semin Perinatol; 1990 Dec 14; 14(6):439-45. PubMed ID: 1981814
    [No Abstract] [Full Text] [Related]

  • 18. The clinical applications of DNA polymorphisms.
    Thein SL, Wainscoat JS.
    Dis Markers; 1986 Oct 14; 4(3):203-18. PubMed ID: 2898316
    [No Abstract] [Full Text] [Related]

  • 19. How to find a mutation behind an inherited disease.
    Peltonen L, Pulkkinen L.
    Ann Clin Res; 1986 Oct 14; 18(5-6):224-30. PubMed ID: 2882725
    [Abstract] [Full Text] [Related]

  • 20. Possibilities and problems in genomic diagnosis of Duchenne muscular dystrophy with molecular probes.
    Speer A, Davies K, McGlade S, Hanke R, Spiegler AW, Szibor R, Sommer D, Herrmann F, Coutelle C.
    Biomed Biochim Acta; 1986 Oct 14; 45(7):K19-27. PubMed ID: 2878658
    [Abstract] [Full Text] [Related]

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