Diagnosis and molecular characterization of a novel α 0 -thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

Int J Lab Hematol. 2017 Oct;39(5):e124-e126. doi: 10.1111/ijlh.12690. Epub 2017 Jun 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Anemia, Hypochromic / genetics*
  • Anemia, Hypochromic / pathology
  • Base Sequence*
  • Child, Preschool
  • Female
  • Glycated Hemoglobin A / genetics
  • Greece
  • Hemoglobin A2 / genetics
  • Hemoglobins, Abnormal / genetics*
  • Humans
  • Sequence Deletion*
  • alpha-Thalassemia / genetics*
  • alpha-Thalassemia / pathology
  • beta-Globins / genetics

Substances

  • Glycated Hemoglobin A
  • Hemoglobins, Abnormal
  • beta-Globins
  • Hemoglobin A2