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PUBMED FOR HANDHELDS

Journal Abstract Search

133 related items for PubMed ID: 1173714

  • 21.
    ; . PubMed ID:
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  • 22. Haemoglobin North Shore-Caracas beta 134 (H12) valine replaced by glutamic acid.
    Arends T, Lehmann H, Plowman D, Stathopoulou R.
    FEBS Lett; 1977 Aug 15; 80(2):261-5. PubMed ID: 891976
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  • 23.
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  • 24. 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 15; 50(8):1628-36. PubMed ID: 5097570
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  • 25.
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  • 26. [Hemoglobin San Diego [beta 109(G11) Val leads to Met] in association with erythrocytosis in a Japanese family].
    Ohba Y, Nakatsuji T, Hattori Y, Miwa S, Miyaji T.
    Nihon Ketsueki Gakkai Zasshi; 1982 Nov 15; 45(6):1009-16. PubMed ID: 7158258
    [No Abstract] [Full Text] [Related]

  • 27. Studies of abnormal hemoglobins in western Japan. Frequency of visible hemoglobin variants, and chemical characterization of hemoglobin Sawara (alpha 26Alabeta2) and hemoglobin Mugino (Hb L Ferrara; alpha247Glybeta2).
    Sumida I.
    Jinrui Idengaku Zasshi; 1975 Mar 15; 19(4):343-63. PubMed ID: 1241593
    [No Abstract] [Full Text] [Related]

  • 28.
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  • 29.
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  • 30. Hemoglobinopathies and thalassemias. Abnormalities of hemoglobin structure, function, and synthesis.
    Honig GR.
    Postgrad Med; 1974 May 15; 55(5):77-83. PubMed ID: 4596320
    [No Abstract] [Full Text] [Related]

  • 31. Further characterisation of haemoglobin F Texas I 5 glutamic acid leads to lysine; 136 alanine.
    Ahern EJ, Wiltshire BG, Lehmann H.
    Biochim Biophys Acta; 1972 Jun 22; 271(1):61-4. PubMed ID: 5038699
    [No Abstract] [Full Text] [Related]

  • 32.
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  • 33.
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  • 34.
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  • 35. Hb F-Oakland or alpha 2G gamma I2(26)(B8)Glu----Lys.
    Kleman K, Lubin B, Wilson JB, Kutlar A, Webber BB, Huisman TH.
    Hemoglobin; 1987 Jun 22; 11(2):181-3. PubMed ID: 2442122
    [No Abstract] [Full Text] [Related]

  • 36. Hb Fukuyama [beta 77(EF1)His----Tyr]: a new abnormal hemoglobin discovered in a Japanese.
    Hidaka K, Iuchi I, Miyake K, Nakahara H, Iwakawa G.
    Hemoglobin; 1988 Jun 22; 12(4):391-4. PubMed ID: 3170240
    [No Abstract] [Full Text] [Related]

  • 37. Symposium: Hemoglobinopathies in Japan. 1. Abnormal hemoglobin in Japan. Biochemical and epidemiologic characters of abnormal hemoglobin in Japan.
    Iuchi I.
    Nihon Ketsueki Gakkai Zasshi; 1968 Oct 22; 31(5):842-51. PubMed ID: 5753624
    [No Abstract] [Full Text] [Related]

  • 38. Hemoglobin Chad [alpha 23 (B4) Glu replaced by Lys] discovered in a Japanese with questionable polycythemia.
    Harano T, Harano K, Shibata S, Ueda S, Mori H, Imai K, Yoshida T.
    Hemoglobin; 1983 Oct 22; 7(6):581-4. PubMed ID: 6689417
    [No Abstract] [Full Text] [Related]

  • 39. Haemoglobin Constant Spring--a chain termination mutant?
    Clegg JB, Weatherall DJ, Milner PF.
    Nature; 1971 Dec 10; 234(5328):337-40. PubMed ID: 4944483
    [No Abstract] [Full Text] [Related]

  • 40. [Structure-function relations of abnormal hemoglobins. II].
    Ruckpaul K.
    Dtsch Gesundheitsw; 1969 Jan 23; 24(4):148-56. PubMed ID: 4916948
    [No Abstract] [Full Text] [Related]

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