Characterization and identification of Hb Bart's hydrops fetalis caused by a compound heterozygous mutation -- SEA /-- CR , a novel α 0 -thalassemia deletion

Int J Lab Hematol. 2020 Jun;42(3):e116-e120. doi: 10.1111/ijlh.13154. Epub 2020 Jan 13.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Hemoglobins, Abnormal / genetics*
  • Heterozygote*
  • Humans
  • Hydrops Fetalis* / diagnosis
  • Hydrops Fetalis* / genetics
  • Mutation*
  • Pregnancy
  • Prenatal Diagnosis*
  • alpha-Thalassemia* / diagnosis
  • alpha-Thalassemia* / genetics

Substances

  • Hemoglobins, Abnormal
  • hemoglobin Bart's