Clinical phenotypes of three children with sickle cell disease caused by HbS/Sicilian (δβ)0 -thalassemia deletion

Am J Hematol. 2022 Apr;97(4):E156-E158. doi: 10.1002/ajh.26470. Epub 2022 Jan 26.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Anemia, Sickle Cell* / complications
  • Anemia, Sickle Cell* / genetics
  • Fetal Hemoglobin / genetics
  • Humans
  • Phenotype
  • Thalassemia* / genetics
  • beta-Thalassemia* / genetics

Substances

  • Fetal Hemoglobin