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PUBMED FOR HANDHELDS

Journal Abstract Search


218 related items for PubMed ID: 2576985

  • 1. [DNA diagnosis of hereditary diseases].
    Nihon Rinsho; 1989 May; 47 Suppl():187-476. PubMed ID: 2576985
    [No Abstract] [Full Text] [Related]

  • 2. [Prenatal diagnosis: molecular basis and techniques used in the diagnosis of monogenic hereditary diseases].
    Villegas Martínez A.
    An Med Interna; 1989 May; 6(5):227-9. PubMed ID: 2577487
    [No Abstract] [Full Text] [Related]

  • 3. [Use of DNA restriction fragment length polymorphisms in the diagnosis of genetically determined diseases].
    Zietkiewicz E, Latos-Bieleńska AM, Słomski R.
    Pol Arch Med Wewn; 1985 Oct; 74(4):269-78. PubMed ID: 2907124
    [No Abstract] [Full Text] [Related]

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

  • 5. [Prenatal diagnosis of congenital diseases of metabolism and of chromosomes alterations].
    Saggese R.
    Pediatria (Napoli); 1979 Dec 31; 87(4):631-47. PubMed ID: 400008
    [No Abstract] [Full Text] [Related]

  • 6. Prenatal laboratory diagnosis of hereditary disorders. Amniocentesis and fibroblast tissue culture permit in utero diagnosis of hereditary metabolic disorders.
    Perl DP.
    R I Med J; 1971 Oct 31; 54(10):509-12. PubMed ID: 4255433
    [No Abstract] [Full Text] [Related]

  • 7. [Prenatal diagnosis in clinical practice].
    González-Ramos M.
    Bol Med Hosp Infant Mex; 1974 Oct 31; 31(4):653-63. PubMed ID: 4425550
    [No Abstract] [Full Text] [Related]

  • 8. Gene derepression: possible applications to diagnosis and management of genetic disease.
    Benson PF.
    Guys Hosp Rep; 1973 Oct 31; 122(1-2):91-108. PubMed ID: 4613623
    [No Abstract] [Full Text] [Related]

  • 9. [Prenatal diagnosis of hereditary hemoglobinopathies].
    Cao A, Pirastu M, Rosatelli C.
    Haematologica; 1989 Oct 31; 74(5 Suppl):213-22. PubMed ID: 2574134
    [No Abstract] [Full Text] [Related]

  • 10. Intrauterine diagnosis of congenital and genetic abnormalities.
    Cortner JA.
    J Ark Med Soc; 1972 Nov 31; 69(6):178-81. PubMed ID: 4263777
    [No Abstract] [Full Text] [Related]

  • 11. [Possibilites and limitations in the prenatal diagnosis of genetic diseases].
    Galjaard H, Jahodova M, Niermijer MF.
    Brux Med; 1972 Feb 31; 52(2):109-21. PubMed ID: 4258331
    [No Abstract] [Full Text] [Related]

  • 12. Fetal tissue sampling--indications, techniques, complications, and experience with sampling of fetal skin, liver, and muscle.
    Cadrin C, Golbus MS.
    West J Med; 1993 Sep 31; 159(3):269-72. PubMed ID: 8236968
    [Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of Friedreich ataxia.
    Wallis J, Shaw J, Wilkes D, Farrall M, Williamson R, Chamberlain S, Skare JC, Milunsky A.
    Am J Med Genet; 1989 Nov 31; 34(3):458-61. PubMed ID: 2574535
    [Abstract] [Full Text] [Related]

  • 14. Foetal medicine.
    Bearn AG.
    Trans Med Soc Lond; 1973 Nov 31; 89():160-3. PubMed ID: 4282186
    [No Abstract] [Full Text] [Related]

  • 15. Prenatal genetic diagnosis (second of three parts).
    Milunsky A, Littlefield JW, Kanfer JN, Kolodny EH, Shih VE, Atkins L.
    N Engl J Med; 1970 Dec 24; 283(26):1441-7. PubMed ID: 4098222
    [No Abstract] [Full Text] [Related]

  • 16. [DNA diagnosis of inborn errors of metabolism].
    Maeda S, Shimada K.
    Tanpakushitsu Kakusan Koso; 1988 Apr 24; 33(5):449-56. PubMed ID: 2908392
    [No Abstract] [Full Text] [Related]

  • 17. [Organization of the early prenatal diagnosis of chromosome aberrations and hereditary metabolic diseases].
    Boué A.
    Arch Fr Pediatr; 1974 May 24; 31(5):433-6. PubMed ID: 4441229
    [No Abstract] [Full Text] [Related]

  • 18. [Importance and current possibilities of prenatal diagnosis of genetically conditioned pathologic states].
    Srsen S.
    Cesk Pediatr; 1971 May 24; 26(5):240-2. PubMed ID: 5559528
    [No Abstract] [Full Text] [Related]

  • 19. DNA testing: diagnostic role in single gene conditions.
    Bodurtha J, Lloyd J, Tams L.
    Va Med Q; 1992 May 24; 119(2):95-6. PubMed ID: 1562623
    [No Abstract] [Full Text] [Related]

  • 20. Prenatal diagnosis of hereditary disease and congenital defects.
    Kaback MM.
    Pediatr Ann; 1981 Feb 24; 10(2):22-37. PubMed ID: 7220122
    [No Abstract] [Full Text] [Related]


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