HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

HB S-HB Monroe; a sickle cell-beta-thalassemia syndrome.

AuthorsI Sweeting, B E Serjeant, G R Serjeant, A E Kulozik, B Vetter
JournalHemoglobin (Hemoglobin) Vol. 22 Issue 2 Pg. 153-6 (Mar 1998) ISSN: 0363-0269 [Print] England
PMID9576332 (Publication Type: Journal Article)
Chemical References
  • Codon
  • Hemoglobin, Sickle
  • Hemoglobins, Abnormal
  • hemoglobin Monroe
  • Globins
Topics
  • Adolescent
  • Adult
  • Black People (genetics)
  • Blood Protein Electrophoresis
  • Child
  • Chromatography, High Pressure Liquid
  • Codon (genetics)
  • Female
  • Globins (genetics)
  • Hemoglobin, Sickle (analysis, genetics)
  • Hemoglobins, Abnormal (analysis, genetics)
  • Heterozygote
  • Humans
  • Isoelectric Focusing
  • Jamaica (epidemiology)
  • Male
  • Sickle Cell Trait (complications, genetics)
  • beta-Thalassemia (complications, 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: