International hemoglobin information center: Variants of the alpha chain

This publication has 619 references indexed in Scilit:

• Hemoglobin dhonburi α₂β₂ 126 (H4) Val → Gly: A new unstable β variant producing a β‐thalassemia intermedia phenotype in association with β°‐Thalassemia
  American Journal of Hematology, 1990
• Hb South milwaukee [β105 (G7) leu → Phe]: A newly-identified hemoglobin variant with high oxygen affinity
  American Journal of Hematology, 1990
• Hemoglobin Villejuif [β 123(H1) Thr→lle]: A new variant found in coincidence with polycythemia vera
  American Journal of Hematology, 1989
• Hb Warsaw (β42 Phe → Val): An unstable hemoglobin with decreased oxygen affinity. I. Hematologic and clinical expression
  American Journal of Hematology, 1989
• Hb regina or α₂β₂96(FG3)LEU → VAL: A high oxygen affinity variant discovered by cation‐exchange HPLC
  American Journal of Hematology, 1985
• Hemoglobin Hamilton or α2β211(a8)Val→Ile: A silent β-chain variant detected by triton X-100 acid-urea polyacrylamide gel electrophoresis
  American Journal of Hematology, 1984
• Characterization of hemoglobin Burke [β107 (G9) Gly→Arg]
  Biochemical Genetics, 1976
• Hemoglobin vancouver [α2β2 73(E17) Asp→ Tyr]: Its structure and function
  Journal of Molecular Evolution, 1976
• Thalassemia intermedia caused by heterozygosity for both β-thalassemia and hemoglobin saki [β14 (a11) leu→pro]
  American Journal of Hematology, 1976
• Ethnological significance of hemoglobin α₂β₂ 121 LYS
  American Journal of Physical Anthropology, 1967