These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


290 related items for PubMed ID: 2574134

  • 1. [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]

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

  • 3. Prenatal diagnosis of inherited hemoglobinopathies.
    Cao A, Pirastu M, Rosatelli C.
    Haematologica; 1990 Apr; 75 Suppl 5():169-77. PubMed ID: 1982278
    [No Abstract] [Full Text] [Related]

  • 4. [Prenatal diagnosis of hemoglobinopathies in the 1st and 2nd pregnancy trimesters].
    Ferrari M, Cantù Rajnoldi A, Cremonesi L, Donzelli C, Pietri S, Tedeschi S, Travi M, Nicolini U, Brambati B.
    Pediatr Med Chir; 1984 Apr; 6(6):769-73. PubMed ID: 6545587
    [Abstract] [Full Text] [Related]

  • 5. [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]

  • 6. Molecular biologic diagnosis of the hemoglobinopathies.
    Schwartz E, Surrey S.
    Hosp Pract (Off Ed); 1986 Sep 15; 21(9):163-78. PubMed ID: 3091617
    [No Abstract] [Full Text] [Related]

  • 7. Prenatal diagnosis of hemoglobinopathies in Ontario, Canada.
    Basran RK, Patterson M, Walker L, Nakamura LM, Eng B, Chui DH, Waye JS.
    Ann N Y Acad Sci; 2005 Sep 15; 1054():507-10. PubMed ID: 16339708
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis of beta-thalassaemia and other haemoglobinopathies in India.
    Thakur (Mahadik) C, Vaz F, Banerjee M, Kapadia C, Natrajan PG, Yagnik H, Gangal S.
    Prenat Diagn; 2000 Mar 15; 20(3):194-201. PubMed ID: 10719320
    [Abstract] [Full Text] [Related]

  • 9. Diagnosis of sickle cell anemia and beta-thalassemia with enzymatically amplified DNA and nonradioactive allele-specific oligonucleotide probes.
    Saiki RK, Chang CA, Levenson CH, Warren TC, Boehm CD, Kazazian HH, Erlich HA.
    N Engl J Med; 1988 Sep 01; 319(9):537-41. PubMed ID: 3405266
    [Abstract] [Full Text] [Related]

  • 10. Noninvasive approaches to prenatal diagnosis of hemoglobinopathies using fetal DNA in maternal plasma.
    Lo YM, Chiu RW.
    Hematol Oncol Clin North Am; 2010 Dec 01; 24(6):1179-86. PubMed ID: 21075287
    [Abstract] [Full Text] [Related]

  • 11. [Prenatal diagnosis in a family carrying the fragile X syndrome using recombinant DNA technics].
    Benítez J, Fernández E, Ramos C, Nunes V, del Río E, Baiget M.
    Rev Clin Esp; 1989 Apr 01; 184(7):364-6. PubMed ID: 2570446
    [Abstract] [Full Text] [Related]

  • 12. Prenatal diagnosis of hemoglobinopathies by using polymerase chain reaction and allele-specific oligonucleotide probes.
    Crisan D, Diven WF, Hartle K, Osborne PT, Mason L.
    Clin Chem; 1989 Sep 01; 35(9):1854. PubMed ID: 2673581
    [No Abstract] [Full Text] [Related]

  • 13. Prenatal diagnosis of hemoglobinopathies: the New England approach.
    Alter BP, Orkin SH, Forget BG, Nathan DG.
    Ann N Y Acad Sci; 1980 Sep 01; 344():151-64. PubMed ID: 6930865
    [No Abstract] [Full Text] [Related]

  • 14. Prenatal diagnosis of unusual hemoglobinopathies.
    Kim JH, Lebo RV, Cai SP, Su X, Chung JH, Mentzer WC, Golbus MS.
    Am J Med Genet; 1994 Mar 01; 50(1):15-20. PubMed ID: 8160747
    [Abstract] [Full Text] [Related]

  • 15. Molecular diagnosis of hemoglobinopathies and thalassemia.
    Kan YW, Chang JC.
    Prenat Diagn; 2010 Jul 01; 30(7):608-10. PubMed ID: 20572100
    [No Abstract] [Full Text] [Related]

  • 16. Prenatal diagnosis of inherited hemoglobinopathies.
    Cao A, Rosatelli C, Pirastu M.
    J Genet Hum; 1986 Nov 01; 34(5):413-24. PubMed ID: 3540210
    [Abstract] [Full Text] [Related]

  • 17. Chorionic villus sampling for first trimester diagnosis of beta-thalassaemia. Report of the first South African case.
    Ramsay M, Levin SL, Rosendorff J, Pinto M, Bernstein R.
    S Afr Med J; 1985 Oct 26; 68(9):672-5. PubMed ID: 4060029
    [Abstract] [Full Text] [Related]

  • 18. Prenatal diagnosis of thalassemia and of the hemoglobinopathies; a review.
    Loukopoulos D.
    Hemoglobin; 1985 Oct 26; 9(5):435-59. PubMed ID: 3910616
    [Abstract] [Full Text] [Related]

  • 19. DNA-based prenatal diagnosis of heritable skin diseases.
    Christiano AM, Uitto J.
    Arch Dermatol; 1993 Nov 26; 129(11):1455-9. PubMed ID: 7902070
    [Abstract] [Full Text] [Related]

  • 20. Direct gene analysis of chorionic villi: A possible technique for first-trimester antenatal diagnosis of haemoglobinopathies.
    Williamson R, Eskdale J, Coleman DV, Niazi M, Loeffler FE, Modell BM.
    Lancet; 1981 Nov 21; 2(8256):1125-7. PubMed ID: 6118574
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 15.