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Tropical and Geographical Medicine|March 1, 1975
Long survival in sickle cell anemiaA V Sar, T H HuismanActa Haematologica|January 1, 1997
Levels of Hb A2 in heterozygotes and homozygotes for beta-thalassemia mutations: influence of mutations in the CACCC and ATAAA motifs of the beta-globin gene promoterT H HuismanClinical Chemistry|October 28, 1997
Combinations of beta chain abnormal hemoglobins with each other or with beta-thalassemia determinants with known mutations: influence on phenotypeT H HuismanAmerican Journal of Hematology|June 1, 1983
Percentages of abnormal hemoglobins in adults with a heterozygosity for an alpha-chain and/or a beta-chain variantT H HuismanBailliere'S Clinical Haematology|March 1, 1993
The structure and function of normal and abnormal haemoglobinsT H HuismanHemoglobin|May 1, 1997
Hb E and alpha-thalassemia; variability in the assembly of beta E chain containing tetramersT H HuismanAmerican Journal of Hematology|January 1, 1979
Sickle cell anemia as a syndrome: a review of diagnostic featuresT H HuismanJournal of Chromatography|July 17, 1987
Separation of hemoglobins and hemoglobin chains by high-performance liquid chromatographyT H HuismanActa Haematologica|January 1, 1987
High-performance liquid chromatography as a method to identify haemoglobin abnormalitiesT H HuismanPageof 37