Citations (8)
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Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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H. Landman & T. H. J. Huisman. (1998) Persistent Iron and Folate Deficiency in a Patient with Deletional Hereditary Persistence of Fetal Hemoglobin; the Effect on the Relative Levels of HB F and Gγ Chains and the Corresponding mRNAS. Hemoglobin 22:1, pages 53-63.
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K. Faridah, E. George, R. J. Trent, B. J. Padanilam, H-J. J. Huang & T. H. J. Huisman. (1986) Homozygosity for a New Type of Gγ(Aγδβ)°-Thalassemia in a Malaysian Male. Hemoglobin 10:4, pages 353-363.
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M. B. Gardiner, J. Carver, B. L. Abraham, J. B. Wilson & T. H. J. Huisman. (1982) Further Studies on the Quantitation of the Hemoglobins A, S, C, and F in Newborn Babies with Difffrent Hemoglobinopathies Using High Pressure Liquid Chromatography. Hemoglobin 6:1, pages 1-13.
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Articles from other publishers (4)
Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. WeatherallSwee Lay Thein & William G. Wood. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin
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Martin H. Steinberg, Bernard G. Forget, Douglas R. Higgs & David J. Weatherall. 2010. Disorders of Hemoglobin. Disorders of Hemoglobin
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A. Kutlar, M. B. Gardiner, M. G. Headlee, A. L. Reese, M. P. Cleek, S. Nagle, P. K. Sukumaran & T. H. J. Huisman. (1984) Heterogeneity in the molecular basis of three types of hereditary persistence of fetal hemoglobin and the relative synthesis of the G? and A? types of ? chain. Biochemical Genetics 22:1-2, pages 21-35.
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M.E. Headlee, M.B. Gardiner, A.L. Reese & T.H.J. Huisman. (1983) The distribution of fetal hemoglobin and the types of γ chain in red cell fractions separated by gradient centrifugation from blood of patients with sickle cell anemia and other hemoglobinopathies. Biochemical Medicine 29:3, pages 337-354.
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