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2. Haemoglobin Madrid beta 115 (G17) alanine--proline: an unstable variant associated with haemolytic anaemia. Outeirino J, Casey R, White JM, Lehmann H. Acta Haematol; 1974; 52(1):53-60. PubMed ID: 4212046 [No Abstract] [Full Text] [Related]
3. 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; 42(5):783-91. PubMed ID: 4270478 [No Abstract] [Full Text] [Related]
4. Hemoglobin SO Arabia disease in a black American. Javid J. Am J Med Sci; 1973 Apr; 265(4):266-74. PubMed ID: 4706390 [No Abstract] [Full Text] [Related]
5. A family with three beta-delta-thalassemia homozygotes. Ramot B, Ben-Bassat I, Gafni D, Zaanoon R. Blood; 1970 Feb; 35(2):158-65. PubMed ID: 5414697 [No Abstract] [Full Text] [Related]
6. Hemoglobin sabine beta 91 (F 7) leu → pro. An unstable variant causing severe anemia with inclusion bodies. Schneider RG, Ueda S, Alperin JB, Brimhall B, Jones RT. N Engl J Med; 1969 Apr 03; 280(14):739-45. PubMed ID: 5773354 [No Abstract] [Full Text] [Related]
7. Various aspects of alpha-thalassemia. Lehmann H, Lang A. Ann N Y Acad Sci; 1974 Apr 03; 232(0):152-8. PubMed ID: 4370548 [No Abstract] [Full Text] [Related]
8. A possible subclass of the hereditary persistence of fetal hemoglobin. Huisman TH, Schroeder WA, Adams HR, Shelton JR, Shelton JB, Apell G. Blood; 1970 Jul 03; 36(1):1-9. PubMed ID: 5421741 [No Abstract] [Full Text] [Related]
11. [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 Oct 03; 18(2):145-56. PubMed ID: 4753554 [No Abstract] [Full Text] [Related]
12. 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]
13. Gamma-beta thalassemia: a cause of hemolytic disease of the newborn. Kan YW, Forget BG, Nathan DG. N Engl J Med; 1972 Jan 20; 286(3):129-34. PubMed ID: 5061687 [No Abstract] [Full Text] [Related]
15. Hemoglobinopathies and thalassemias. Abnormalities of hemoglobin structure, function, and synthesis. Honig GR. Postgrad Med; 1974 May 20; 55(5):77-83. PubMed ID: 4596320 [No Abstract] [Full Text] [Related]
16. Beta-thalassaemia and some rare haemoglobin variants in the highlands of Scotland. Cook IA, Lehmann H. Scott Med J; 1973 Jan 20; 18(1):14-20. PubMed ID: 4717660 [No Abstract] [Full Text] [Related]
17. 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 20; 23(4):403-17. PubMed ID: 5084806 [No Abstract] [Full Text] [Related]
18. A new abnormal hemoglobin O Padova, alpha 30 (B11) Glu -- Lys, and a dyserythropoietic anemia with erythroblastic multinuclearity coexisting in the same patient. Vettore L, De Sandre G, Di Iorio EE, Winterhalter KH, Lang A, Lehmann H. Blood; 1974 Dec 20; 44(6):869-77. PubMed ID: 4429803 [No Abstract] [Full Text] [Related]
19. Acquired hemoglobin H disease. Hamilton RW, Schwartz E, Atwater J, Erslev AJ. N Engl J Med; 1971 Nov 25; 285(22):1217-21. PubMed ID: 5113710 [No Abstract] [Full Text] [Related]
20. Hemoglobin G Georgia or alpha 2-95 Leu (G-2) beta-2. Huisman TH, Adams HR, Wilson JB, Efremov GD, Reynolds CA, Wrightstone RN. Biochim Biophys Acta; 1970 Mar 31; 200(3):578-80. PubMed ID: 5436649 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]