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Journal Abstract Search

349 related items for PubMed ID: 6291506

  • 1. Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.
    Felice AE, Ozdonmez R, Headlee ME, Huisman TH.
    Biochem Genet; 1982 Aug; 20(7-8):689-701. PubMed ID: 6291506
    [No Abstract] [Full Text] [Related]

  • 2. Haemoglobin GPhiladelphia and its interaction with haemoglobin S and alpha-thalassaemia in Nigerians.
    Knox-Macaulay HH, Fleming AF, Lamb J, Mba EC.
    Clin Lab Haematol; 1984 Aug; 6(2):113-21. PubMed ID: 6488738
    [Abstract] [Full Text] [Related]

  • 3. A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.
    Steinberg MH, Coleman MB, Adams JG, Hartmann RC, Saba H, Anagnou NP.
    Blood; 1986 Feb; 67(2):469-73. PubMed ID: 3942832
    [Abstract] [Full Text] [Related]

  • 4. Modification of hemoglobin H disease by sickle trait.
    Matthay KK, Mentzer WC, Dozy AM, Kan YW, Bainton DF.
    J Clin Invest; 1979 Oct; 64(4):1024-32. PubMed ID: 479366
    [Abstract] [Full Text] [Related]

  • 5. Hemoglobin constitution of double heterozygotes for alpha or beta-thalassemia and Hb J Sardegna.
    Maccioni L, Galanello R, Melis MA, Cao A.
    Hemoglobin; 1984 Oct; 8(5):497-507. PubMed ID: 6548732
    [Abstract] [Full Text] [Related]

  • 6. (delta beta) zero thalassemia of the Southern Italian type. Its geographical origin and interaction with the sickle cell gene.
    Trent RJ, Svirklys L, Harris MG, Hocking DR, Kronenberg H.
    Pathology; 1986 Jan; 18(1):117-22. PubMed ID: 2425331
    [Abstract] [Full Text] [Related]

  • 7. Globin synthesis studies in a person heterozygous for alpha-thalassemia-2, Hb S and Hb G Philadelphia.
    Ballas SK, Walker BK, Atwater J.
    Clin Chim Acta; 1980 Jan 01; 100(1):1-6. PubMed ID: 7351073
    [Abstract] [Full Text] [Related]

  • 8. The association of Hb Stanleyville II with alpha thalassemia and Hb S.
    Costa FF, Zago MA, Sonati MF, Bottura C.
    Nouv Rev Fr Hematol (1978); 1987 Jan 01; 29(6):387-90. PubMed ID: 3452204
    [Abstract] [Full Text] [Related]

  • 9. Evidence for posttranslational control of Hb C synthesis in an individual with Hb C trait and alpha-thalassemia.
    Liebhaber SA, Cash FE, Cornfield DB.
    Blood; 1988 Feb 01; 71(2):502-4. PubMed ID: 3337909
    [Abstract] [Full Text] [Related]

  • 10. The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia.
    Milner PF, Garbutt GJ, Nolan-Davis LV, Jonah F, Wilson LB, Wilson JT.
    Am J Hematol; 1986 Apr 01; 21(4):383-95. PubMed ID: 2420172
    [Abstract] [Full Text] [Related]

  • 11. The proportion of hybrid heterodimers in homozygous or doubly heterozygous beta chain variant hemoglobinopathies associated with alpha chain hemoglobin variants.
    Krauss JS.
    Ann Clin Lab Sci; 2000 Oct 01; 30(4):391-4. PubMed ID: 11045763
    [Abstract] [Full Text] [Related]

  • 12. Alpha-thalassemia and the production of different alpha chain variants in heterozygotes.
    Felice AE, Webber BB, Huisman TH.
    Biochem Genet; 1981 Jun 01; 19(5-6):487-98. PubMed ID: 7295286
    [Abstract] [Full Text] [Related]

  • 13. Hemoglobins in Togolese newborns: Hb S, Hb C, Hb Bart's, and alpha-globin gene status.
    Segbena AY, Prehu C, Wajcman H, Bardakdjian-Michau J, Messie K, Feteke L, Vovor A, David M, Feingold J, Galacteros F.
    Am J Hematol; 1998 Nov 01; 59(3):208-13. PubMed ID: 9798658
    [Abstract] [Full Text] [Related]

  • 14. Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb S.
    Codrington JF, Codrington FA, Wisse JH, Wilson JB, Webber BB, Wong SC, Huisman TH.
    Hemoglobin; 1989 Nov 01; 13(6):543-56. PubMed ID: 2606723
    [Abstract] [Full Text] [Related]

  • 15. Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.
    Honig GR, Gunay U, Mason RG, Vida LN, Ferenc C.
    Pediatr Res; 1976 Jun 01; 10(6):613-20. PubMed ID: 1272638
    [Abstract] [Full Text] [Related]

  • 16. Mapping the alpha-globin genes in Hb J Mexico carriers.
    Trabuchet G, Morle F, Verdier G, Godet J, Benabadji M, Nigon VM.
    Hum Genet; 1982 Jun 01; 62(2):164-6. PubMed ID: 6298095
    [Abstract] [Full Text] [Related]

  • 17. A new variant, HB Muscat [alpha 2 beta (2)32(B14)Leu----Val] observed in association with HB S in an Arabian family.
    Ramachandran M, Gu LH, Wilson JB, Kitundu MN, Adekile AD, Liu JC, McKie KM, Huisman TH.
    Hemoglobin; 1992 Jun 01; 16(4):259-66. PubMed ID: 1517102
    [Abstract] [Full Text] [Related]

  • 18. Sickle cell disease caused by Hb S/Québec-CHORI: treatment with hydroxyurea and response.
    Tubman VN, Bennett CM, Luo HY, Chui DH, Heeney MM.
    Pediatr Blood Cancer; 2007 Aug 01; 49(2):207-10. PubMed ID: 17551985
    [Abstract] [Full Text] [Related]

  • 19. Molecular exclusion of haemoglobin SD disease by prenatal diagnosis.
    Fodor FH, Eng CM.
    Prenat Diagn; 1999 Jan 01; 19(1):58-60. PubMed ID: 10073909
    [Abstract] [Full Text] [Related]

  • 20. Usefulness of HPLC methodology for the characterization of combinations of the common beta chain variants Hbs S, C, and O-Arab, and the alpha chain variant Hb G-Philadelphia.
    Kutlar F, Kutlar A, Nuguid E, Prchal J, Huisman TH.
    Hemoglobin; 1993 Feb 01; 17(1):55-66. PubMed ID: 8454470
    [Abstract] [Full Text] [Related]

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