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

N Engl J Med. 1991 Oct 17;325(16):1150-4. doi: 10.1056/NEJM199110173251607.
No abstract available

Publication types

  • Case Reports
  • 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.

MeSH terms

  • Anemia, Sickle Cell / etiology*
  • Child, Preschool
  • Chromatography, High Pressure Liquid
  • Female
  • Hemoglobins, Abnormal / analysis*
  • Heterozygote
  • Humans
  • Isoelectric Focusing
  • Polymers
  • Sickle Cell Trait / blood*
  • Sickle Cell Trait / genetics

Substances

  • Hemoglobins, Abnormal
  • Polymers
  • hemoglobin Quebec-Chori