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Sickle cell disease in a patient with sickle cell trait and compound heterozygosity for hemoglobin S and hemoglobin Quebec-Chori.

AuthorsH E Witkowska, B H Lubin, Y Beuzard, S Baruchel, D W Esseltine, E P Vichinsky, K M Kleman, J Bardakdjian-Michau, L Pinkoski, S Cahn
JournalThe New England journal of medicine (N Engl J Med) Vol. 325 Issue 16 Pg. 1150-4 (Oct 17 1991) ISSN: 0028-4793 [Print] United States
PMID1891024 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Hemoglobins, Abnormal
  • Polymers
  • hemoglobin Quebec-Chori
Topics
  • Anemia, Sickle Cell (etiology)
  • Child, Preschool
  • Chromatography, High Pressure Liquid
  • Female
  • Hemoglobins, Abnormal (analysis)
  • Heterozygote
  • Humans
  • Isoelectric Focusing
  • Polymers
  • Sickle Cell Trait (blood, genetics)

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