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PUBMED FOR HANDHELDS

Journal Abstract Search


190 related items for PubMed ID: 1562623

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

  • 2. [Noninvasive prenatal diagnosis of single gene disorders through cell-free fetal DNA in maternal blood].
    Guo QW, Zhou YL.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):410-3. PubMed ID: 20017305
    [Abstract] [Full Text] [Related]

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  • 5. [New frontiers in noninvasive, prenatal screening and diagnosis: fetal DNA circulating in maternal blood].
    Montagnana M, Lippi G, Guidi GC.
    Minerva Ginecol; 2007 Jun; 59(3):331-41. PubMed ID: 17576408
    [Abstract] [Full Text] [Related]

  • 6. [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]

  • 7. [Prenatal diagnosis of genetic diseases. Preliminary results].
    Velázquez A, Lowenberg-Favela E, Del Veccio N, Carnevale A, Niño de Rivera O, Castillo J.
    Ginecol Obstet Mex; 1978 Nov; 44(265):395-400. PubMed ID: 738615
    [No Abstract] [Full Text] [Related]

  • 8. Recent advances in non-invasive prenatal DNA diagnosis through analysis of maternal blood.
    Sekizawa A, Purwosunu Y, Matsuoka R, Koide K, Okazaki S, Farina A, Saito H, Okai T.
    J Obstet Gynaecol Res; 2007 Dec; 33(6):747-64. PubMed ID: 18001438
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  • 9. [Presymptomatic and prenatal laboratory diagnosis of hereditary diseases using the DNA analysis method (review of the literature)].
    Mzhel'skaia TI, Larskiĭ EG, Milovidov IuK.
    Lab Delo; 1991 Dec; (12):3-10. PubMed ID: 1724484
    [No Abstract] [Full Text] [Related]

  • 10. [Current status and trends of prenatal gene diagnosis].
    Ren Z, Zeng Y.
    Zhonghua Fu Chan Ke Za Zhi; 1997 Nov; 32(11):643-5. PubMed ID: 9639760
    [No Abstract] [Full Text] [Related]

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

  • 12. Cell-free fetal DNA and non-invasive prenatal diagnosis.
    Rafi I, Chitty L.
    Br J Gen Pract; 2009 May; 59(562):e146-8. PubMed ID: 19401007
    [No Abstract] [Full Text] [Related]

  • 13. [Revision of the diagnostics of endangered pregnancies and the need for regular and systematic discussion/counseling].
    Horváth E.
    Orv Hetil; 2000 Nov 19; 141(47):2577-8. PubMed ID: 11186430
    [No Abstract] [Full Text] [Related]

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  • 15. [Prenatal (predelivery) diagnosis of hereditary diseases and congenital developmental defects in the fetus].
    Bakharev VA, Karetnikova NA.
    Feldsher Akush; 1987 Oct 19; 52(10):21-3. PubMed ID: 3436446
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  • 17. [Use of DNA polymorphism in the diagnosis of human genetic diseases].
    Cebrat S.
    Postepy Hig Med Dosw; 1988 Oct 19; 42(5):461-82. PubMed ID: 2908211
    [No Abstract] [Full Text] [Related]

  • 18. [Prenatal diagnosis by the presence of fetal DNA in maternal blood].
    Penchaszadeh VB.
    Arch Argent Pediatr; 2009 Oct 19; 107(5):392-4. PubMed ID: 19809758
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  • 20. [Prenatal diagnosis of genetic anomalies].
    González-Ramos M.
    Ginecol Obstet Mex; 1972 Feb 19; 31(184):131-7. PubMed ID: 5059734
    [No Abstract] [Full Text] [Related]


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