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2. Sickle cell-beta +-thalassaemia: a haematological and clinical study in Liberia. Bienzle U; Kappes R; Reimer A; Feldheim M; Tischendorf FW; Kohne E Blut; 1983 Nov; 47(5):279-85. PubMed ID: 6194836 [TBL] [Abstract][Full Text] [Related]
3. Clinical and haematological evaluation of beta thalassaemia intermedia characterised by unusually low Hb F and increased Hb A2: beta thalassaemia intermedia II. Gurgey A; Kayin S; Kansu E; Altay C J Med Genet; 1985 Jun; 22(3):213-21. PubMed ID: 2409284 [TBL] [Abstract][Full Text] [Related]
4. The importance of the genetic picture and globin synthesis in determining the clinical and haematological features of thalassaemia intermedia. Gallo E; Massaro P; Miniero R; David D; Tarella C Br J Haematol; 1979 Feb; 41(2):211-21. PubMed ID: 427031 [TBL] [Abstract][Full Text] [Related]
5. The heterogeneity of normal Hb A2-beta thalassaemia in Greece. Kattamis C; Metaxotou-Mavromati A; Wood WG; Nash JR; Weatherall DJ Br J Haematol; 1979 May; 42(1):109-23. PubMed ID: 465353 [TBL] [Abstract][Full Text] [Related]
6. Clinical and haematological evaluation of beta thalassaemia intermedia with increased Hb F and Hb A2 in heterozygotes: beta thalassaemia intermedia I. Altay C; Gurgey A J Med Genet; 1985 Jun; 22(3):205-12. PubMed ID: 2409283 [TBL] [Abstract][Full Text] [Related]
7. The Negro variety of hereditary persistence of fetal haemoglobin is a mild form of thalassaemia. Charache S; Clegg JB; Weatherall DJ Br J Haematol; 1976 Dec; 34(4):527-34. PubMed ID: 990187 [TBL] [Abstract][Full Text] [Related]
8. Heterogeneity of beta thalassaemia in Thailand. Yenchitsomanus P; Baramee A; Fucharoen S; Pootrakul P; Wasi P Southeast Asian J Trop Med Public Health; 1982 Dec; 13(4):618-27. PubMed ID: 6189197 [TBL] [Abstract][Full Text] [Related]
9. Beta + thalassemia--Portuguese type: clinical, haematological and molecular studies of a newly defined form of beta thalassaemia. Tamagnini GP; Lopes MC; Castanheira ME; Wainscoat JS; Wood WG Br J Haematol; 1983 Jun; 54(2):189-200. PubMed ID: 6189507 [TBL] [Abstract][Full Text] [Related]
10. Homozygous beta thalassemia in American Blacks: the problem of mild thalassemia. Braverman AS; McCurdy PR; Manos O; Sherman A J Lab Clin Med; 1973 Jun; 81(6):857-66. PubMed ID: 4122857 [No Abstract] [Full Text] [Related]
11. Alpha-thalassaemia trait in various racial groups in the United Kingdom: characterization of a variant of alpha-thalassaemia in Indians. Walford DM; Deacon R Br J Haematol; 1976 Oct; 34(2):193-206. PubMed ID: 974033 [TBL] [Abstract][Full Text] [Related]
12. The haemoglobin pattern of sickle cell and haemoglobin C beta +-thalassaemia in Liberia. Willcox M J Med Genet; 1983 Dec; 20(6):430-2. PubMed ID: 6655669 [TBL] [Abstract][Full Text] [Related]
13. Inclusion-body beta-thalassemia trait. A form of beta thalassemia producing clinical manifestations in simple heterozygotes. Stamatoyannopoulos G; Woodson R; Papayannopoulou T; Heywood D; Kurachi S N Engl J Med; 1974 Apr; 290(17):939-43. PubMed ID: 4361439 [No Abstract] [Full Text] [Related]
14. A comparison of the homozygous states for G gamma and G gamma A gamma delta beta thalassaemia. Amin AB; Pandya NL; Diwin PP; Darbre PD; Kattamis C; Metaxatou-Mavromati A; White JM; Wood WG; Clegg JB; Weatherall DJ Br J Haematol; 1979 Dec; 43(4):537-48. PubMed ID: 93489 [TBL] [Abstract][Full Text] [Related]
16. Thalassaemia in northern Liberia. A survey in the Mount Nimba area. Willcox MC J Med Genet; 1975 Mar; 12(1):55-63. PubMed ID: 1121021 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Five families with homozygous delta-thalassaemia in Japan. Yasukawa M; Saito S; Fujita S; Ohta Y; Ikeda K; Matsumoto I; Kobayashi Y Br J Haematol; 1980 Oct; 46(2):199-206. PubMed ID: 6158985 [TBL] [Abstract][Full Text] [Related]
19. The silent carrier of beta thalassemia. Schwartz E N Engl J Med; 1969 Dec; 281(24):1327-33. PubMed ID: 5355437 [No Abstract] [Full Text] [Related]
20. A form of hereditary persistence of fetal haemoglobin characterized by uneven cellular distribution of haemoglobin F and the production of haemoglobins A and A2 in homozygotes. Weatherall DJ; Cartner R; Clegg JB; Wood WG; Macrae IA; Mackenzie A Br J Haematol; 1975 Feb; 29(2):205-20. PubMed ID: 811241 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]