Molecular analysis of deletion and nondeletion hereditary persistence of fetal hemoglobin and identification of a new mutation causing beta-thalassemia

Ann N Y Acad Sci. 1985:445:159-69. doi: 10.1111/j.1749-6632.1985.tb17185.x.
No abstract available

Publication types

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

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Chromosome Deletion*
  • Chromosome Mapping
  • DNA / genetics
  • DNA Restriction Enzymes
  • Fetal Hemoglobin / genetics*
  • Fetal Hemoglobin / metabolism
  • Greece
  • Mice
  • Mutation*
  • Thalassemia / genetics*
  • Transfection

Substances

  • DNA
  • Fetal Hemoglobin
  • DNA Restriction Enzymes