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25. Compound heterozygosity of non-deletional hereditary persistence of fetal hemoglobin and deltabeta-thalassemia. Kalamaras A; Chassanidis C; Samara M; Papadakis MN; Vagena A; Aleporou-Marinou V; Patrinos GP; Kollia P Am J Hematol; 2008 Sep; 83(9):760. PubMed ID: 18615450 [No Abstract] [Full Text] [Related]
26. Control of homozygous beta-thalassemia by carrier screening and antenatal diagnosis in Sardinia. Cao A; Furbetta M; Galanello R; Melis MA; Angius A; Rosatelli C; Ruggeri R; Addis M; Tuveri T; Falchi AM; Maccioni L; Paglietti E; Scalas MT Birth Defects Orig Artic Ser; 1982; 18(7):303-11. PubMed ID: 7159738 [No Abstract] [Full Text] [Related]
27. The gradual understanding of thalassemia. Lehmann H Prog Clin Biol Res; 1984; 165():121-36. PubMed ID: 6209728 [No Abstract] [Full Text] [Related]
28. 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]
29. [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]
30. Community control of thalassemia as a model of genetic disease: experience in the Lombardy region of Italy. Masera G; Ferrari M Birth Defects Orig Artic Ser; 1988; 23(5B):443-8. PubMed ID: 3390573 [No Abstract] [Full Text] [Related]
31. The diagnosis of the thalassaemia carrier state. Cauchi MN; Smith MB Aust Fam Physician; 1979 Jun; 8(6):676-7, 679, 84. PubMed ID: 464920 [No Abstract] [Full Text] [Related]
32. 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]
33. Prevention of thalassemia in the Ferrara area. Vullo C; Lucci M; Salsini G; Toffoli C; Ravani A; Dolcini B; Venturoli A; Bardi A; Conigli P Haematologica; 1990; 75 Suppl 5():142-52. PubMed ID: 2086374 [No Abstract] [Full Text] [Related]
34. Cultural and psychosocial considerations in screening for thalassemia in the Southeast Asian refugee population. Nidorf JF; Ngo KY Am J Med Genet; 1993 Jun; 46(4):398-402. PubMed ID: 8357011 [TBL] [Abstract][Full Text] [Related]
35. A simple non radioactive method for detecting beta-thalassemia/hbe disease: application to prenatal diagnosis. Fucharoen S; Fucharoen G; Ratanasiri T; Jetsrisuparb A; Fukumaki Y Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():278-81. PubMed ID: 8629124 [TBL] [Abstract][Full Text] [Related]
36. The frequent occurrence of alpha thalassemia in blacks. Dozy AM; Embury SH; Kan YW Trans Assoc Am Physicians; 1979; 92():96-103. PubMed ID: 232948 [No Abstract] [Full Text] [Related]
37. [Genetic diagnosis of alpha and beta thalassemia dual heterozygote]. Zeng R; Yu S; Hu B Zhonghua Xue Ye Xue Za Zhi; 1998 Oct; 19(10):525-7. PubMed ID: 11189497 [TBL] [Abstract][Full Text] [Related]
38. Prenatal diagnosis of hemoglobinopathies in Ontario, Canada. Basran RK; Patterson M; Walker L; Nakamura LM; Eng B; Chui DH; Waye JS Ann N Y Acad Sci; 2005; 1054():507-10. PubMed ID: 16339708 [TBL] [Abstract][Full Text] [Related]
39. Molecular pathology of alpha-thalassemia. Liebhaber SA; Kan YW Birth Defects Orig Artic Ser; 1982; 18(7):35-44. PubMed ID: 6760927 [No Abstract] [Full Text] [Related]
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