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Journal Abstract Search

408 related items for PubMed ID: 6407302

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

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

  • 3. Of mice and men.
    Tolstoshev P.
    Nature; 1978 Nov 02; 276(5683):13-5. PubMed ID: 105291
    [No Abstract] [Full Text] [Related]

  • 4. [Molecular bases of thalassemia].
    Labie D, Troungos C, Wajcman H.
    Ann Med Interne (Paris); 1985 Nov 02; 136(4):323-45. PubMed ID: 2412477
    [No Abstract] [Full Text] [Related]

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  • 7. Antenatal diagnosis of severe beta thalassemia during the first trimester of pregnancy.
    Trent RJ, Anderson J, Boogert T, Kronenberg H.
    Pathology; 1985 Oct 02; 17(4):568-72. PubMed ID: 3005951
    [Abstract] [Full Text] [Related]

  • 8. The intrauterine diagnosis of hemoglobin disorders.
    Wong SC, Ali MA, Benzie R.
    Clin Perinatol; 1984 Jun 02; 11(2):283-308. PubMed ID: 6086205
    [Abstract] [Full Text] [Related]

  • 9. [Structure of the globin genes in persons with anomalous hemoglobins].
    Kavsan VM.
    Tsitol Genet; 1982 Jun 02; 16(2):62-72. PubMed ID: 6179278
    [No Abstract] [Full Text] [Related]

  • 10. Detection and gene defects in the thalassemias and related disorders.
    Bank A, Mears JG, Ramirez F, Burns AL, Feldenzer J, Spence S.
    Ann N Y Acad Sci; 1980 Jun 02; 344():1-11. PubMed ID: 6249170
    [No Abstract] [Full Text] [Related]

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  • 12. Molecular genetics of human hemoglobin synthesis.
    Forget BG.
    Ann Intern Med; 1979 Oct 02; 91(4):605-16. PubMed ID: 384860
    [Abstract] [Full Text] [Related]

  • 13. The molecular biology of the thalassemia syndromes.
    Bank A, Ramirez F.
    CRC Crit Rev Biochem; 1978 Oct 02; 5(4):343-67. PubMed ID: 363354
    [No Abstract] [Full Text] [Related]

  • 14. Genetic and molecular diversity in nondeletion Hb H disease.
    Higgs DR, Pressley L, Aldridge B, Clegg JB, Weatherall DJ, Cao A, Hadjiminas MG, Kattamis C, Metaxatou-Mavromati A, Rachmilewitz EA, Sophocleous T.
    Proc Natl Acad Sci U S A; 1981 Sep 02; 78(9):5833-7. PubMed ID: 6272319
    [Abstract] [Full Text] [Related]

  • 15. Update in the genetics of thalassemia: What clinicians need to know.
    Shang X, Xu X.
    Best Pract Res Clin Obstet Gynaecol; 2017 Feb 02; 39():3-15. PubMed ID: 27876354
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. Disorders of human hemoglobin.
    Bank A, Mears JG, Ramirez F.
    Science; 1980 Feb 01; 207(4430):486-93. PubMed ID: 7352255
    [Abstract] [Full Text] [Related]

  • 18.
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  • 19. Polymorphism and molecular pathology of the human beta-globin gene.
    Orkin SH, Antonarakis SE, Kazazian HH.
    Prog Hematol; 1983 Feb 01; 13():49-73. PubMed ID: 6366914
    [No Abstract] [Full Text] [Related]

  • 20. Molecular pathology of alpha-thalassemia.
    Kan YW.
    Ann N Y Acad Sci; 1985 Feb 01; 445():28-36. PubMed ID: 3860131
    [Abstract] [Full Text] [Related]

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