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22. [Beta-thalassemia mutations and single nucleotide polymorphism at -158 of Ggamma-globin gene associated with altered levels of Hb F in beta-thalassemia heterozygotes]. Chen JF; Long GF; Lin WX; Chen P Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):498-501. PubMed ID: 15476181 [TBL] [Abstract][Full Text] [Related]
23. Flow cytometric measurement of hemoglobin F in RBCs: diagnostic usefulness in the distinction of hereditary persistence of fetal hemoglobin (HPFH) and hemoglobin S-hPFH from other conditions with elevated levels of hemoglobin F. Hoyer JD; Penz CS; Fairbanks VF; Hanson CA; Katzmann JA Am J Clin Pathol; 2002 Jun; 117(6):857-63. PubMed ID: 12047136 [TBL] [Abstract][Full Text] [Related]
24. Hemoglobin switch in the newborn: a flow cytometry analysis. Amoyal I; Fibach E Neonatology; 2007; 91(1):61-8. PubMed ID: 17344654 [TBL] [Abstract][Full Text] [Related]
25. Genotypic heterogeneity and correlation to intergenic haplotype within high HbF beta-thalassemia intermedia. Papachatzopoulou A; Kourakli A; Makropoulou P; Kakagianne T; Sgourou A; Papadakis M; Athanassiadou A Eur J Haematol; 2006 Apr; 76(4):322-30. PubMed ID: 16519704 [TBL] [Abstract][Full Text] [Related]
26. [Heterozygous beta thalassemia with increased HbF: independent segregation of beta thalassemia and hereditary persistent fetal hemoglobin (Swiss type) in a Spanish family]. De Blas JM; Martín E; Martínez ML; Caso F Sangre (Barc); 1985; 30(1):28-36. PubMed ID: 2408346 [No Abstract] [Full Text] [Related]
27. Beta-thalassemia with exceptionally high hemoglobin A2. Differential expression of the delta-globin gene in the presence of beta-thalassemia. Steinberg MH; Coleman MB; Adams JG J Lab Clin Med; 1982 Oct; 100(4):548-57. PubMed ID: 6288819 [TBL] [Abstract][Full Text] [Related]
28. [Heterozygous beta-thalassemia without icrease of hemoglobin A2]. Marti HR; Grieder HR Schweiz Med Wochenschr; 1970 Apr; 100(15):663-6. PubMed ID: 5438669 [No Abstract] [Full Text] [Related]
29. Allele-specific transcription of fetal genes in primary erythroid cell cultures from Lepore and deltabeta degrees thalassemia patients. Di Marzo R; Acuto S; Calzolari R; Maggio A Exp Hematol; 2005 Nov; 33(11):1363-70. PubMed ID: 16263421 [TBL] [Abstract][Full Text] [Related]
30. Haematological and clinical data in 200 cases of thalassaemia trait in eastern Spain. Vayá A; Carratalá A; Martinez C; Aznar J Nouv Rev Fr Hematol (1978); 1983; 25(6):369-73. PubMed ID: 6198618 [TBL] [Abstract][Full Text] [Related]
31. [Hemolytic disease of the newborn and chronic hypochromic microcytic anemia in one family: gamma-delta-beta thalassemia]. Oort M; Heerspink W; Roos D; Bernini LF Tijdschr Kindergeneeskd; 1981 Dec; 49(6):199-207. PubMed ID: 7330840 [TBL] [Abstract][Full Text] [Related]
32. The molecular basis of normal HbA2 (type 2) beta-thalassemia in Greece. Tzetis M; Traeger-Synodinos J; Kanavakis E; Metaxotou-Mavromati A; Kattamis C Hematol Pathol; 1994; 8(1-2):25-34. PubMed ID: 8034555 [TBL] [Abstract][Full Text] [Related]
33. Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations. Sebastiani P; Wang L; Nolan VG; Melista E; Ma Q; Baldwin CT; Steinberg MH Am J Hematol; 2008 Mar; 83(3):189-95. PubMed ID: 17918249 [TBL] [Abstract][Full Text] [Related]
34. Alpha thalassaemia and the haematology of normal Jamaican children. Maude GH; Higgs DR; Beckford M; Grandison Y; Mason K; Taylor B; Serjeant BE; Serjeant GR Clin Lab Haematol; 1985; 7(4):289-95. PubMed ID: 2420505 [TBL] [Abstract][Full Text] [Related]
35. The HBS1L-MYB intergenic region on chromosome 6q23 is a quantitative trait locus controlling fetal haemoglobin level in carriers of beta-thalassaemia. So CC; Song YQ; Tsang ST; Tang LF; Chan AY; Ma ES; Chan LC J Med Genet; 2008 Nov; 45(11):745-51. PubMed ID: 18697826 [TBL] [Abstract][Full Text] [Related]
36. [Thalassemia minor in families of German descent in the Bergische Land (author's transl)]. Streit W MMW Munch Med Wochenschr; 1977 Feb; 119(7):215-8. PubMed ID: 403446 [TBL] [Abstract][Full Text] [Related]
37. Prevalence of hemoglobinopathies in north Jordan. Bashir N; Barkawi M; Sharif L; Momani A; Gharaibeh N Trop Geogr Med; 1992 Jan; 44(1-2):122-5. PubMed ID: 1379763 [TBL] [Abstract][Full Text] [Related]
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39. Haemolytic disease of the newborn and chronic anaemia induced by gamma beta thalassaemia in a Dutch family. Oort M; Heerspink W; Roos D; Flavell RA; Bernini LF Br J Haematol; 1981 Jun; 48(2):251-62. PubMed ID: 7195273 [TBL] [Abstract][Full Text] [Related]
40. Prospective study of red blood cell indices, hemoglobin A2, and hemoglobin F in infants heterozygous for Beta-thalassemia. Galanello R; Melis MA; Ruggeri R; Cao A J Pediatr; 1981 Jul; 99(1):105-8. PubMed ID: 6166735 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]