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8. Role of haemichromes in the formation of inclusion bodies in haemoglobin H disease. Rachmilewitz EA, Peisach J, Bradley TB, Blumberg WE. Nature; 1969 Apr 19; 222(5190):248-50. PubMed ID: 4305116 [No Abstract] [Full Text] [Related]
10. [The micro-ovalocytosis. Hematologic and genetic study of a family group with 3 affected members]. Nenci GG, Migliorini E, Santeusanio F, Casamassima F, Gambelunghe C. Haematologica; 1967 Apr 19; 52(10):775-813. PubMed ID: 4976164 [No Abstract] [Full Text] [Related]
14. Molecular pathology of thalassemia syndromes. Marks PA, Bank A. Fed Proc; 1971 Apr 19; 30(3):977-82. PubMed ID: 5575303 [No Abstract] [Full Text] [Related]
15. Congenital inclusion body hemolytic anemia: study of a family. Ben-Bassat I, Brok-Simoni F, Benyaminov M, Danon D, Ramot B. Isr J Med Sci; 1969 Apr 19; 5(3):383-94. PubMed ID: 5822147 [No Abstract] [Full Text] [Related]
16. Hemoglobin-Seattle (alpha-2 beta-2 76-Glu): an unstable hemoglobin causing chronic hemolytic anemia. Huehns ER, Hecht F, Yoshida A, Stamatoyannopoulos G, Hartman J, Motulsky AG. Blood; 1970 Aug 19; 36(2):209-18. PubMed ID: 5427455 [No Abstract] [Full Text] [Related]