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T H Huisman

Showing results (11-20 of 646) with videos related to

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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 Huisman
FEBS Letters|October 1, 1978
The hemoglobin P-Galveston-Hb-C conduction in members of a black family from South CarolinaT H Huisman
Bailliere'S Clinical Haematology|March 1, 1993
The structure and function of normal and abnormal haemoglobinsT H Huisman
Hemoglobin|May 1, 1997
Hb E and alpha-thalassemia; variability in the assembly of beta E chain containing tetramersT H Huisman
Hemoglobin|May 1, 1997
Compound heterozygosity for Hb S and the hybrid HbS Lepore, P-Nilotic, and Kenya; comparison of hematological and hemoglobin composition dataT H Huisman
British Journal of Haematology|August 1, 1990
Frequencies of common beta-thalassaemia alleles among different populations: variability in clinical severityT H Huisman
Pediatrics|May 1, 1989
Usefulness of cation exchange high performance liquid chromatography as a testing procedureT H Huisman
American Journal of Hematology|January 1, 1979
Sickle cell anemia as a syndrome: a review of diagnostic featuresT H Huisman
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1972
Chromatographic separation of hemoglobins A 2 and C. The quantities of hemoglobin A 2 in patients with AC trait, CC disease, and C- -thalassemiaT H Huisman
Advances in Clinical Chemistry|January 1, 1972
Normal and abnormal human hemoglobinsT H Huisman
Pageof 65

Showing results (11-20 of 646) with videos related to

Sort By:
Pageof 65
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 Huisman
FEBS Letters|October 1, 1978
The hemoglobin P-Galveston-Hb-C conduction in members of a black family from South CarolinaT H Huisman
Bailliere'S Clinical Haematology|March 1, 1993
The structure and function of normal and abnormal haemoglobinsT H Huisman
Hemoglobin|May 1, 1997
Hb E and alpha-thalassemia; variability in the assembly of beta E chain containing tetramersT H Huisman
Hemoglobin|May 1, 1997
Compound heterozygosity for Hb S and the hybrid HbS Lepore, P-Nilotic, and Kenya; comparison of hematological and hemoglobin composition dataT H Huisman
British Journal of Haematology|August 1, 1990
Frequencies of common beta-thalassaemia alleles among different populations: variability in clinical severityT H Huisman
Pediatrics|May 1, 1989
Usefulness of cation exchange high performance liquid chromatography as a testing procedureT H Huisman
American Journal of Hematology|January 1, 1979
Sickle cell anemia as a syndrome: a review of diagnostic featuresT H Huisman
Clinica Chimica Acta; International Journal of Clinical Chemistry|August 1, 1972
Chromatographic separation of hemoglobins A 2 and C. The quantities of hemoglobin A 2 in patients with AC trait, CC disease, and C- -thalassemiaT H Huisman
Advances in Clinical Chemistry|January 1, 1972
Normal and abnormal human hemoglobinsT H Huisman
Pageof 65