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Journal Abstract Search

234 related items for PubMed ID: 2907124

  • 1. [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]

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

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

  • 5. Experience of a molecular genetics service in prenatal diagnosis by DNA analysis.
    Trent RJ, Volpato F, Wallace RC, Lindeman R, Yakas J.
    Pathology; 1990 Jul; 22(3):165-8. PubMed ID: 2243730
    [Abstract] [Full Text] [Related]

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  • 8. Antenatal diagnosis.
    Old JM, Ludlam CA.
    Baillieres Clin Haematol; 1991 Apr; 4(2):391-428. PubMed ID: 1680511
    [No Abstract] [Full Text] [Related]

  • 9. Antenatal monitoring of genetic disorders.
    Simpson JL.
    Clin Obstet Gynaecol; 1979 Aug; 6(2):259-93. PubMed ID: 387326
    [No Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis. Fetoscopy.
    Nicolaides K, Rodeck CH.
    Br J Hosp Med; 1984 Jun; 31(6):396-405. PubMed ID: 6430373
    [Abstract] [Full Text] [Related]

  • 11. Genetic diseases: diagnosis by restriction endonuclease analysis.
    Antonarakis SE, Phillips JA, Kazazian HH.
    J Pediatr; 1982 Jun; 100(6):845-56. PubMed ID: 6283049
    [Abstract] [Full Text] [Related]

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

  • 13. The use of amniocentesis for prenatal genetic counseling.
    Gertner M, Hsu LY, Martin J, Hirshhorn K.
    Bull N Y Acad Med; 1970 Nov; 46(11):916-21. PubMed ID: 5273905
    [No Abstract] [Full Text] [Related]

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

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  • 18. Noninvasive approaches to prenatal diagnosis of hemoglobinopathies using fetal DNA in maternal plasma.
    Lo YM, Chiu RW.
    Hematol Oncol Clin North Am; 2010 Dec; 24(6):1179-86. PubMed ID: 21075287
    [Abstract] [Full Text] [Related]

  • 19. [Prenatal diagnosis of hereditary diseases (a review of the literature)].
    Sviatkina OB, Kun'kina LZ.
    Akush Ginekol (Mosk); 1973 Apr; 49(4):11-5. PubMed ID: 4616633
    [No Abstract] [Full Text] [Related]

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