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alpha-globin gene deletions associated with Hb J Tongariki.

Abstract
Three identical alpha + thalassemia genes, one of which always carried the Hb J Tongariki mutation, have been observed in Vanuatuans. Despite the fact that at least two of them have arisen by different types of crossover event, the expression of all three haplotypes is identical.
AuthorsD K Bowden, L Pressley, D R Higgs, J B Clegg, D J Weatherall
JournalBritish journal of haematology (Br J Haematol) Vol. 51 Issue 2 Pg. 243-9 (Jun 1982) ISSN: 0007-1048 [Print] England
PMID6979350 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Hemoglobins, Abnormal
  • Hemoglobin J
  • Globins
  • DNA
  • hemoglobin J Tongariki
Topics
  • Chromosome Deletion
  • Chromosomes, Human, 16-18
  • DNA
  • Genes
  • Globins (genetics)
  • Hemoglobin J (genetics)
  • Hemoglobins, Abnormal (genetics)
  • Humans
  • Pedigree
  • Phenotype
  • Thalassemia (genetics)
  • Vanuatu

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