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Journal Abstract Search

287 related items for PubMed ID: 1148221

  • 1. Hemoglobin-A2-Coburg or alpha2delta2116Arg leads to His (G18).
    Sharma RS, Williams L, Wilson JB, Huisman TH.
    Biochim Biophys Acta; 1975 Jun 26; 393(2):379-82. PubMed ID: 1148221
    [Abstract] [Full Text] [Related]

  • 2. [A2' (B2) hemoglobin associated with beta thalassemia and hereditary persistence of fetal hemoglobin. Study in 3 Colombian families].
    Echavarria A, Molina C, Zapata CI.
    Sangre (Barc); 1973 Jun 26; 18(2):145-56. PubMed ID: 4753554
    [No Abstract] [Full Text] [Related]

  • 3. An individual with "Miyada"-like hemoglobin indistinguishable from hemoglobin A2.
    Schroeder WA, Huisman TH, Hyman C, Shelton JR, Apell G.
    Biochem Genet; 1973 Oct 26; 10(2):135-47. PubMed ID: 4750742
    [No Abstract] [Full Text] [Related]

  • 4.
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    [No Abstract] [Full Text] [Related]

  • 5. Hemoglobin O arab in four negro families and its interaction with hemoglobin S and hemoglobin C.
    Milner PF, Miller C, Grey R, Seakins M, DeJong WW, Went LN.
    N Engl J Med; 1970 Dec 24; 283(26):1417-25. PubMed ID: 5481775
    [No Abstract] [Full Text] [Related]

  • 6. A homozygote for the Hb G type of foetal haemoglobin in India: a study of two Indian and four Negro families.
    Sukumaran PK, Huisman TH, Schroeder WA, McCurdy PR, Freehafer JT, Bouver N, Shelton JR, Shelton JB, Apell G.
    Br J Haematol; 1972 Oct 24; 23(4):403-17. PubMed ID: 5084806
    [No Abstract] [Full Text] [Related]

  • 7. [Hemoglobinopathies and thalassemias].
    Oort M, Roos D.
    Ned Tijdschr Geneeskd; 1982 Jul 03; 126(27):1234-7. PubMed ID: 7121623
    [No Abstract] [Full Text] [Related]

  • 8. An unusual hemoglobin anomaly and its relation to alpha-thalassemia and hemoglobin-H disease.
    Efremov GD, Wrightstone RN, Huisman TH, Schroeder WA, Hyman C, Ortega J, Williams K.
    J Clin Invest; 1971 Aug 03; 50(8):1628-36. PubMed ID: 5097570
    [Abstract] [Full Text] [Related]

  • 9. On the structure of the hemoglobins A, A2, and F in a Negro with homozygous beta-thalassemia.
    Schroeder WA, Huisman TH, Shelton JR, Apell G, Shelton JB, Brodie AR, Lutcher CL, Blunt MH, Miller A.
    Biochem Med; 1974 Jul 03; 10(3):276-92. PubMed ID: 4835407
    [No Abstract] [Full Text] [Related]

  • 10. The interaction of alpha-thalassaemia and haemoglobin G Philadelphia.
    Rieder RF, Woodbury DH, Rucknagel DL.
    Br J Haematol; 1976 Feb 03; 32(2):159-65. PubMed ID: 1247489
    [Abstract] [Full Text] [Related]

  • 11. The molecular basis of hemoglobin disease.
    Stamatoyannopoulos G.
    Annu Rev Genet; 1972 Feb 03; 6():47-70. PubMed ID: 4581487
    [No Abstract] [Full Text] [Related]

  • 12. Duplicated alpha-chain genes in Hopkins-2 haemoglobin of man and evidence for unequal crossing over between them.
    Ostertag W, von Ehrenstein G, Charache S.
    Nat New Biol; 1972 May 17; 237(72):90-4. PubMed ID: 4503919
    [No Abstract] [Full Text] [Related]

  • 13. The interaction of hemoglobin E with beta thalassemia: a study of hemoglobin synthesis in a family of mixed Burmese and Iranian origin.
    Feldman R, Rieder RF.
    Blood; 1973 Nov 17; 42(5):783-91. PubMed ID: 4270478
    [No Abstract] [Full Text] [Related]

  • 14. The genetics of alpha-thalassemia in Yemenite and Iraqi Jews.
    Zaizov R, Kirschmann C, Matoth Y, Adam A.
    Isr J Med Sci; 1973 Nov 17; 9(9):1457-60. PubMed ID: 4775132
    [No Abstract] [Full Text] [Related]

  • 15. Chemical heterogeneity of foetal haemoglobin in the Lepore haemoglobinopathy.
    Efremov GD, Sadikario A, Stojmirovic E, Schroeder WA, Shelton JR, Shelton JB, Apell G, Wilson JB, Brodie AR, Huisman TH.
    Br J Haematol; 1974 Jun 17; 27(2):319-29. PubMed ID: 4846463
    [No Abstract] [Full Text] [Related]

  • 16. A new sickling disorder resulting from interaction of the genes for haemoglobin S and alpha-thalassaemia.
    Weatherall DJ, Clegg JB, Blankson J, McNeil JR.
    Br J Haematol; 1969 Dec 17; 17(6):517-26. PubMed ID: 5357741
    [No Abstract] [Full Text] [Related]

  • 17. [Heterozygous beta-thalassemia without icrease of hemoglobin A2].
    Marti HR, Grieder HR.
    Schweiz Med Wochenschr; 1970 Apr 11; 100(15):663-6. PubMed ID: 5438669
    [No Abstract] [Full Text] [Related]

  • 18. Double heterozygosity for hemoglobin G (alpha-2 68Lys beta-A2) and hemoglobin D (alpha A2-beta-121Gln).
    Rothman MC, Ranney HM.
    Blood; 1971 Feb 11; 37(2):177-83. PubMed ID: 5549195
    [No Abstract] [Full Text] [Related]

  • 19. Hereditary persistence of foetal haemoglobin associated with a gamma beta fusion variant, haemoglobin Kenya.
    Clegg JB, Weatherall DJ, Gilles HM.
    Nat New Biol; 1973 Dec 12; 246(154):184-6. PubMed ID: 4519001
    [No Abstract] [Full Text] [Related]

  • 20. Chromatographic separation of hemoglobins A 2 and C. The quantities of hemoglobin A 2 in patients with AC trait, CC disease, and C- -thalassemia.
    Huisman TH.
    Clin Chim Acta; 1972 Aug 12; 40(1):159-63. PubMed ID: 5056624
    [No Abstract] [Full Text] [Related]

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