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PUBMED FOR HANDHELDS

Journal Abstract Search

330 related items for PubMed ID: 6297633

  • 1. Prenatal diagnosis by DNA analysis.
    Kan YW, Chang JC, Dozy AM.
    Birth Defects Orig Artic Ser; 1982; 18(7):275-83. PubMed ID: 6297633
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  • 2. Prenatal diagnosis using DNA polymorphisms. Report on 95 pregnancies at risk for sickle-cell disease or beta-thalassemia.
    Boehm CD, Antonarakis SE, Phillips JA, Stetten G, Kazazian HH.
    N Engl J Med; 1983 May 05; 308(18):1054-8. PubMed ID: 6300677
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  • 7. DNA analysis as clinical investigation: when and how?
    Jeanpierre M, Junien C.
    Ann Genet; 1984 May 05; 27(3):134-47. PubMed ID: 6095729
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  • 8. [DNA analysis by polymerase chain reaction].
    Hattori Y.
    Rinsho Byori; 1992 Jun 05; 40(6):607-16. PubMed ID: 1325004
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  • 10. Improved detection of the sickle mutation by DNA analysis: application to prenatal diagnosis.
    Orkin SH, Little PF, Kazazian HH, Boehm CD.
    N Engl J Med; 1982 Jul 01; 307(1):32-6. PubMed ID: 6176867
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  • 12. A sensitive test for prenatal diagnosis of sickle cell anemia: direct analysis of amniocyte DNA with MstII.
    Chang JC, Kan YW.
    Trans Assoc Am Physicians; 1982 Jul 01; 95():71-8. PubMed ID: 6304979
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  • 13. Prenatal diagnosis of hemoglobinopathies.
    Nathan DG, Alter BP, Orkin SH.
    Clin Perinatol; 1979 Sep 01; 6(2):275-91. PubMed ID: 391466
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  • 16. Detection of sickle cell anaemia and thalassaemias.
    Chehab FF, Doherty M, Cai SP, Kan YW, Cooper S, Rubin EM.
    Nature; 1979 Sep 01; 329(6137):293-4. PubMed ID: 3627274
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  • 19. [The significance of hemoglobinopathies in pregnancy].
    Landman H, Visser GH.
    Ned Tijdschr Geneeskd; 1984 Jun 23; 128(25):1191-5. PubMed ID: 6462266
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  • 20. Prenatal diagnosis of sickle syndromes in India: dilemmas in counselling.
    Colah R, Surve R, Nadkarni A, Gorakshakar A, Phanasgaonkar S, Satoskar P, Mohanty D.
    Prenat Diagn; 2005 May 23; 25(5):345-9. PubMed ID: 15906420
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