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American 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 HuismanAmerican Journal of Human Genetics|July 1, 1976
Hb Grady and alpha thalassemia: a contribution to the problem of the number of Hb alpha structural loci in manT H Huisman, A MillerHemoglobin|January 1, 1984
Hemoglobin abnormalities in a black family with HB S, hereditary persistence of HB F, and a gamma chain variant; a reevaluation through gene mappingT Harano, T H HuismanHemoglobin|January 1, 1981
The frequency of the A gamma T gene in the presence and absence of the beta S or beta C gene in the Black population of the Southeastern USAT H Huisman, B WebberPageof 83