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2. SURVIVAL OF 51 CR-LABELLED RED CELLS IN SUBJECTS WITH THALASSAEMIA-TRAIT OR G6PD DEFICIENCY OR BOTH ABNORMALITIES. BERNINI L; LATTE B; SINISCALCO M; PIOMELLI S; SPADA U; ADINOLFI M; MOLLISON PL Br J Haematol; 1964 Apr; 10():171-80. PubMed ID: 14141616 [No Abstract] [Full Text] [Related]
3. HAEMOGLOBIN NICOSIA. AN ALPHA-CHAIN VARIANT AND ITS COMBINATION WITH BETA-THALASSAEMIA. FESSAS C; KARAKLIS A; LOUKOPOULOS D; STAMATOYANNOPOULOS G; FESSAS P Br J Haematol; 1965 May; 11():323-30. PubMed ID: 14282069 [No Abstract] [Full Text] [Related]
4. Some problems of hemoglobin patterns in different thalassemic syndromes showing the heterogeneity of beta-thalassemia genes. Aksoy M; Erdem S Ann N Y Acad Sci; 1969 Nov; 165(1):13-24. PubMed ID: 5260139 [No Abstract] [Full Text] [Related]
5. F-Thalassemia. A study of thirty-one families with simple heterozygotes and combinations of F-Thalassemia with A2-Thalassemia. Stamatoyannopoulos G; Fessas P; Papayannopoulou T Am J Med; 1969 Aug; 47(2):194-208. PubMed ID: 5808240 [No Abstract] [Full Text] [Related]
6. Studies on beta thalassemia trait in pregnancy. Pakes JB; Cooperberg AA; Gelfand MM Am J Obstet Gynecol; 1970 Dec; 108(8):1217-23. PubMed ID: 5482859 [No Abstract] [Full Text] [Related]
7. HAEMOGLOBINOPATHIES IN THAILAND. II. INCIDENCE AND DISTRIBUTION OF ELEVATIONS OF HAEMOGLOBIN A2 AND HAEMOGLOBIN F; A SURVEY OF 2790 PEOPLE. FLATZ G; PIK C; SRINGAM S Br J Haematol; 1965 Mar; 11():227-36. PubMed ID: 14262182 [No Abstract] [Full Text] [Related]
8. THE IRON-BINDING CAPACITY OF THALASSEMIC INDIVIDUALS. HAMPE OG; DAROCHA FJ Acta Genet Med Gemellol (Roma); 1964 Oct; 13():418-22. PubMed ID: 14247243 [No Abstract] [Full Text] [Related]
9. [RELATIONS BETWEEN HEMOGLOBIN A2 AND HEMOGLOBIN F IN PATIENTS WITH THALASSEMIA]. SCHETTINI F; MELONI T Haematologica; 1964; 49():471-87. PubMed ID: 14213263 [No Abstract] [Full Text] [Related]
10. GENETIC CONTROL OF HEMOGLOBIN A2 SYNTHESIS: AN UNUSUAL HEREDITARY PATTERN IN A FAMILY WITH THALASSEMIA TRAIT. LEE GR; HAUT A; CARTWRIGHT GE; WINTROBE MM J Lab Clin Med; 1964 Jul; 64():72-8. PubMed ID: 14192570 [No Abstract] [Full Text] [Related]
11. Haemoglobin E-beta-thalassaemia; a study of eight cases in Northwest India. Ghosh K; Chakrabarty AK; Mohanty D; Das KC Trop Geogr Med; 1983 Sep; 35(3):267-71. PubMed ID: 6196886 [TBL] [Abstract][Full Text] [Related]
12. 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]
14. [A CASE OF MICRODREPANOCYTIC DISEASE DUE TO S HEMOGLOBIN AND A VARIETY OF MICROCYTHEMIA WITH NORMAL QUOTA OF A2 HEMOGLOBIN AND ELEVATED QUOTA OF F HEMOGLOBIN (THIRD VARIETY OF MICRODREPANOCYTIC DISEASE)]. SILVESTRONI E; BIANCO I Prog Med (Napoli); 1964 Aug; 20():509-13. PubMed ID: 14235120 [No Abstract] [Full Text] [Related]
15. [PRESENCE OF MICROCYTHEMIA WITH NORMAL AMOUNT OF HEMOGLOBIN A2 AND ELEVATED AMOUNT OF HEMOGLOBIN F IN A CALABRIAN FAMILY (THIRD VARIETY OF MICROCYTHEMIA)]. SILVESTRONI E; BIANCO I; BRANCATI C Policlinico Prat; 1964 Oct; 71():1543-5. PubMed ID: 14213722 [No Abstract] [Full Text] [Related]
16. ERYTHROCYTE LIFE-SPAN AND SITES OF DESTRUCTION IN THALASSEMIA MAJOR. RELATION TO CLINICAL AND LABORATORY FINDINGS. SITARZ AL; ULTMANN JE; WOLFF JA Acta Haematol; 1963; 30():204-14. PubMed ID: 14107559 [No Abstract] [Full Text] [Related]
17. A VARIANT OF HEMOGLOBIN A2 FOUND IN A NEGRO FAMILY. LEE RC; HUISMAN TH Blood; 1964 Nov; 24():495-501. PubMed ID: 14236725 [No Abstract] [Full Text] [Related]
18. THE SPHERE OF INFLUENCE OF THE BETA-THALASSEMIA MUTATION. COMINGS DE; CONLEY CL Blood; 1963 Aug; 22():234-6. PubMed ID: 14045307 [No Abstract] [Full Text] [Related]
19. [PROBLEMS OF CHARACTERIZATION OF THE THALASSEMIC TRAIT]. LUPI L Pediatria (Napoli); 1963; 71():952-61. PubMed ID: 14125500 [No Abstract] [Full Text] [Related]