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Organization of alpha-chain genes among Hb G-Philadelphia heterozygotes in association with Hb S, beta-thalassemia, and alpha-thalassemia-2.

AuthorsA E Felice, R Ozdonmez, M E Headlee, T H Huisman
JournalBiochemical genetics (Biochem Genet) Vol. 20 Issue 7-8 Pg. 689-701 (Aug 1982) ISSN: 0006-2928 [Print] United States
PMID6291506 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Hemoglobin, Sickle
  • Hemoglobins, Abnormal
  • Globins
  • DNA
  • Hemoglobin C
  • hemoglobin G Philadelphia
  • DNA Restriction Enzymes
Topics
  • Adult
  • Anemia, Sickle Cell (genetics)
  • DNA (analysis)
  • DNA Restriction Enzymes
  • Genes
  • Globins (genetics)
  • Hemoglobin C (genetics)
  • Hemoglobin C Disease (genetics)
  • Hemoglobin, Sickle (genetics)
  • Hemoglobins, Abnormal (genetics)
  • Heterozygote
  • Humans
  • Infant, Newborn
  • Nucleic Acid Hybridization
  • Thalassemia (genetics)

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