These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
144 related articles for article (PubMed ID: 990187)
21. Biosynthetic studies and gamma-chain composition in the Greek type of hereditary persistence of fetal hemoglobin and in its association with beta-thalassemia. Camaschella C; Ciocca-Vasino MA; Guerrasio A; Balegno G; Barberis E; Delponte D; Saglio G Acta Haematol; 1979; 61(5):272-7. PubMed ID: 111454 [TBL] [Abstract][Full Text] [Related]
22. Globin chain synthesis in Hb J Baltimore-beta (+)-thalassemia. Ballas SK; Atwater J; Theriault C; Kim HC; Propst M Am J Clin Pathol; 1981 Jun; 75(6):843-6. PubMed ID: 6167160 [TBL] [Abstract][Full Text] [Related]
23. Negro alpha-thalassaemia is caused by deletion of a single alpha-globin gene. Higgs DR; Pressley L; Old JM; Hunt DM; Clegg JB; Weatherall DJ; Serjeant GR Lancet; 1979 Aug; 2(8137):272-6. PubMed ID: 88608 [TBL] [Abstract][Full Text] [Related]
25. Association of heterocellular HPFH, beta(+)-thalassaemia, and delta beta(0)-thalassaemia: haematological and molecular aspects. Cianetti L; Care A; Sposi NM; Giampaolo A; Calandrini M; Petrini M; Massa A; Marinucci M; Mavilio F; Ceccanti M J Med Genet; 1984 Aug; 21(4):263-7. PubMed ID: 6208362 [TBL] [Abstract][Full Text] [Related]
26. Interaction of two different disorders in the beta-globin gene cluster associated with an increased hemoglobin F production: a novel deletion type of (G) gamma + ((A) gamma delta beta)(0)-thalassemia and a delta(0)-hereditary persistence of fetal hemoglobin determinant. Losekoot M; Fodde R; Gerritsen EJ; van de Kuit I; Schreuder A; Giordano PC; Vossen JM; Bernini LF Blood; 1991 Feb; 77(4):861-7. PubMed ID: 1704267 [TBL] [Abstract][Full Text] [Related]
27. G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C. Higgs DR; Clegg JB; Wood WG; Weatherall DJ J Med Genet; 1979 Aug; 16(4):288-95. PubMed ID: 490582 [TBL] [Abstract][Full Text] [Related]
28. Heterozygous beta-thalassaemia with normal haemoglobin pattern. Haematologic, haemoglobin and biosynthesis study of 4 families. Silvestroni E; Bianco I; Graziani B; Carboni C Acta Haematol; 1978; 59(6):332-40. PubMed ID: 97891 [TBL] [Abstract][Full Text] [Related]
29. 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]
30. Heterocellular hereditary persistence of fetal haemoglobin (heterocellular HPFH) and its interaction with beta thalassaemia. Wood WG; Weatherall DJ; Clegg JB; Hamblin TJ; Edwards JH; Barlow AM Br J Haematol; 1977 Aug; 36(4):461-73. PubMed ID: 889715 [No Abstract] [Full Text] [Related]
31. 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]
32. 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]
33. Greek (A gamma) variant of hereditary persistence of fetal haemoglobin: globin gene organization and studies of expression of fetal haemoglobins in clonal erythroid cultures. Papayannopoulou T; Lawn RM; Stamatoyannopoulos G; Maniatis T Br J Haematol; 1982 Mar; 50(3):387-99. PubMed ID: 6175332 [TBL] [Abstract][Full Text] [Related]
34. 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]
35. The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassemia, various forms of hereditary persistence of fetal hemoglobin, normal adults and newborn. Huisman TH; Efremov GD; Reese AL; Howard JS; Gravely ME; Harris HF; Wilson JB Hemoglobin; 1979; 3(4):223-52. PubMed ID: 500369 [TBL] [Abstract][Full Text] [Related]
37. Globin chain synthesis in beta-thalassemia with normal hemoglobins A2 and F. Aksoy M; Almiş G; Bermek E Hemoglobin; 1979; 3(4):263-70. PubMed ID: 500371 [TBL] [Abstract][Full Text] [Related]