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43. 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]
44. Types of thalassemia in Sicily. Russo G Birth Defects Orig Artic Ser; 1982; 18(7):185-8. PubMed ID: 7159728 [No Abstract] [Full Text] [Related]
46. [Heterozygote beta-microcythemic children in Iesi. Statistical findings and health prospects]. Bini PL; Beccaceci P; Carotti G; Binci MC Minerva Med; 1983 Dec; 74(49-50):2921-5. PubMed ID: 6664585 [No Abstract] [Full Text] [Related]
47. [Mediterranean hemopathy in Puglia. Hematological, biochemical and genetic aspects. Study of 96 families]. Putignano A Quad Sclavo Diagn; 1972 Sep; 8(3):737-84. PubMed ID: 4671793 [No Abstract] [Full Text] [Related]
48. [Polymorphism of human fetal hemoglobin. II. Incidence of the A-gamma(75) Ileu-replaced-by-thr globin chain in the Spanish population and in various thalassemic syndromes]. Baiget M; Colls M; De Pablos JM; Aventin A; Del Río E; Gimferrer E Sangre (Barc); 1983; 28(5):551-6. PubMed ID: 6198735 [No Abstract] [Full Text] [Related]
49. Rapid high-performance liquid chromatographic method for the separation of the three types of gamma-chain of human fetal haemoglobin. Baudin V; Wajcman H J Chromatogr; 1984 Sep; 299(2):495-7. PubMed ID: 6209293 [No Abstract] [Full Text] [Related]
50. Preventation of thalassemia in Australia. Hendy J Southeast Asian J Trop Med Public Health; 1999; 30 Suppl 2():94-6. PubMed ID: 11400797 [TBL] [Abstract][Full Text] [Related]
51. Survey of Haryana children for abnormal hemoglobins. Aggarwal VP; Dhatt PS; Singh H Indian Pediatr; 1983 Apr; 20(4):255-8. PubMed ID: 6194111 [No Abstract] [Full Text] [Related]
52. A multicenter trial of the effectiveness of zeta-globin enzyme-linked immunosorbent assay and hemoglobin H inclusion body screening for the detection of alpha0-thalassemia trait. Lafferty JD; Barth DS; Sheridan BL; McFarlane AG; Halchuk LM; Raby A; Crowther MA Am J Clin Pathol; 2008 Feb; 129(2):309-15. PubMed ID: 18208812 [TBL] [Abstract][Full Text] [Related]
53. Molecular characterization of HbH disease in the Cuban population. Martinez G; Ferreira R; Hernandez A; Di Rienzo A; Felicetti L; Colombo B Hum Genet; 1986 Apr; 72(4):318-9. PubMed ID: 3009300 [TBL] [Abstract][Full Text] [Related]
54. The cellular distribution of fetal hemoglobin: normal adults and hemoglobinopathies. Dover GJ; Boyer SH Tex Rep Biol Med; 1980-1981; 40():43-54. PubMed ID: 6172872 [No Abstract] [Full Text] [Related]
55. [Alpha- and beta-thalassemia genotypes in the Po delta]. Del Senno L; Bernardi F; Busin M; Marchetti G; Perrotta C; Conconi F; Capellozza G; Vullo C Minerva Med; 1981 Mar; 72(11):684-9. PubMed ID: 7243014 [No Abstract] [Full Text] [Related]
56. A newly defined X linked mental retardation syndrome associated with alpha thalassaemia. Gibbons RJ; Wilkie AO; Weatherall DJ; Higgs DR J Med Genet; 1991 Nov; 28(11):729-33. PubMed ID: 1770527 [No Abstract] [Full Text] [Related]
57. Genotypes of alpha-thalassemia in the Chinese. Huang YW; Wang RX; Zhang NJ; Yang XY; Guo XZ; Li CQ; Zhang J; Liang X; Zhang JW; Wu GY Birth Defects Orig Artic Ser; 1987; 23(5A):31-8. PubMed ID: 3689913 [No Abstract] [Full Text] [Related]