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3. [Double heterozygote HbC-beta(O) thalassemia. A new case of this combination in a Caucasian subject]. Vives Corrons JL, Vallespí MT, Jou JM, Aguilar i Basocompte JL. Sangre (Barc); 1983; 28(5):656-62. PubMed ID: 6665699 [No Abstract] [Full Text] [Related]
11. Sickle cell syndromes. III. Silent-carrier alpha-thalassemia in combination with hemoglobin S and hemoglobin C. Honig GR, Mason RG, Tremaine LM, Vida LN. Pediatr Res; 1979 Oct; 13(10):1109-11. PubMed ID: 503635 [Abstract] [Full Text] [Related]
12. Ultrastructural abnormalities and arrest of protein biosynthesis in some erythroblasts from homozygotes for haemoglobin C and double heterozygotes for haemoglobin C and beta-thalassaemia. Wickramasinghe SN. Clin Lab Haematol; 1990 Oct; 12(4):401-8. PubMed ID: 2081381 [Abstract] [Full Text] [Related]
16. Anemia in pregnancy. Scott DE, Pritchard JA. Clin Perinatol; 1974 Sep; 1(2):491-506. PubMed ID: 4620160 [No Abstract] [Full Text] [Related]
17. Obstetric care for women with thalassemia. Lao TT. Best Pract Res Clin Obstet Gynaecol; 2017 Feb; 39():89-100. PubMed ID: 28341055 [Abstract] [Full Text] [Related]
18. Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family. Horányi M, Szelényi J, Rona G, Lang A, Lehmann H, Hollán SR. Folia Haematol Int Mag Klin Morphol Blutforsch; 1980 Feb; 107(4):654-60. PubMed ID: 6162733 [Abstract] [Full Text] [Related]