HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Homozygous delta-thalassemia first discovered in Japanese family with hereditary persistence of fetal hemoglobin.

AuthorsY Ota, K Yamaoka, I Sumida, S Fujita, T Fujimura
JournalBlood (Blood) Vol. 37 Issue 6 Pg. 706-15 (Jun 1971) ISSN: 0006-4971 [Print] United States
PMID5162313 (Publication Type: Journal Article)
Chemical References
  • Fetal Hemoglobin
  • Iron
Topics
  • Adult
  • Anemia, Hypochromic (complications, drug therapy)
  • Chromatography, Ion Exchange
  • Electrophoresis, Starch Gel
  • Erythrocytes (cytology)
  • Female
  • Fetal Hemoglobin (analysis)
  • Heterozygote
  • Homozygote
  • Humans
  • Iron (therapeutic use)
  • Japan
  • Male
  • Osmotic Fragility
  • Pedigree
  • Thalassemia (blood, diagnosis, genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: