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Journal Abstract Search

172 related items for PubMed ID: 2412477

  • 1. [Molecular bases of thalassemia].
    Labie D, Troungos C, Wajcman H.
    Ann Med Interne (Paris); 1985; 136(4):323-45. PubMed ID: 2412477
    [No Abstract] [Full Text] [Related]

  • 2. The intrauterine diagnosis of hemoglobin disorders.
    Wong SC, Ali MA, Benzie R.
    Clin Perinatol; 1984 Jun; 11(2):283-308. PubMed ID: 6086205
    [Abstract] [Full Text] [Related]

  • 3. Thalassemia.
    Poncz M, Cohen A, Schwartz E.
    Adv Pediatr; 1984 Jun; 31():43-86. PubMed ID: 6516946
    [No Abstract] [Full Text] [Related]

  • 4. The mutational basis of the thalassemia syndromes.
    Kazazian HH, Cho S, Phillips JA.
    Prog Med Genet; 1977 Jun; 2():165-204. PubMed ID: 897199
    [No Abstract] [Full Text] [Related]

  • 5.
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  • 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. [Structure of the globin genes in persons with anomalous hemoglobins].
    Kavsan VM.
    Tsitol Genet; 1982 Sep 15; 16(2):62-72. PubMed ID: 6179278
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
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  • 9. Antenatal diagnosis of severe beta thalassemia during the first trimester of pregnancy.
    Trent RJ, Anderson J, Boogert T, Kronenberg H.
    Pathology; 1985 Oct 15; 17(4):568-72. PubMed ID: 3005951
    [Abstract] [Full Text] [Related]

  • 10. Prenatal diagnosis of the fetus at risk for beta-thalassemia/hemoglobin E disease: a report of the first case in Thailand.
    Kanokpongsakdi S, Winichagoon P, Fucharoen S, Manassagorn J, Tanphaichitr V.
    J Med Assoc Thai; 1987 Jan 15; 70(1):38-43. PubMed ID: 3572289
    [No Abstract] [Full Text] [Related]

  • 11. The molecular genetics of human hemoglobins.
    Maniatis T, Fritsch EF, Lauer J, Lawn RM.
    Annu Rev Genet; 1980 Jan 15; 14():145-78. PubMed ID: 6452087
    [No Abstract] [Full Text] [Related]

  • 12. The thalassemia syndromes.
    Weatherall DJ.
    Tex Rep Biol Med; 1980 Jan 15; 40():323-33. PubMed ID: 7034274
    [No Abstract] [Full Text] [Related]

  • 13. The molecular genetics of thalassemia.
    Orkin SH, Nathan DG.
    Adv Hum Genet; 1981 Jan 15; 11():233-80. PubMed ID: 6267910
    [No Abstract] [Full Text] [Related]

  • 14. Haemoglobinopathies.
    Old J.
    Prenat Diagn; 1996 Dec 15; 16(13):1181-6. PubMed ID: 9061749
    [Abstract] [Full Text] [Related]

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

  • 16. Analysis of fetal blood using capillary electrophoresis system: a simple method for prenatal diagnosis of severe thalassemia diseases.
    Srivorakun H, Fucharoen G, Sae-Ung N, Sanchaisuriya K, Ratanasiri T, Fucharoen S.
    Eur J Haematol; 2009 Jul 15; 83(1):57-65. PubMed ID: 19226360
    [Abstract] [Full Text] [Related]

  • 17. Prenatal diagnosis of inherited hemoglobinopathies.
    Cao A, Rosatelli C, Pirastu M.
    J Genet Hum; 1986 Nov 15; 34(5):413-24. PubMed ID: 3540210
    [Abstract] [Full Text] [Related]

  • 18. Thalassemia intermedia associated with the Hb Constant Spring EE Bart's disease in pregnancy: a molecular and hematological analysis.
    Fucharoen S, Fucharoen G, Sae-ung N, Sanchaisuriya K.
    Blood Cells Mol Dis; 2007 Nov 15; 39(2):195-8. PubMed ID: 17587614
    [Abstract] [Full Text] [Related]

  • 19. [Genetics of human hemoglobin and its molecular disorders].
    Cohen-Solal M.
    Biochimie; 1981 Feb 15; 63(2):III-VIII. PubMed ID: 6164402
    [No Abstract] [Full Text] [Related]

  • 20. The thalassemias: molecular mechanisms of human genetic disease.
    Spritz RA, Forget BG.
    Am J Hum Genet; 1983 May 15; 35(3):333-61. PubMed ID: 6407302
    [No Abstract] [Full Text] [Related]

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