Heterozygosity at the alpha-haptoglobin locus associated with a deletion, 16q22 leads to 16qter

Cytogenet Cell Genet. 1978;22(1-6):513. doi: 10.1159/000131011.
No abstract available

MeSH terms

  • Child
  • Chromosome Deletion*
  • Chromosome Mapping*
  • Chromosomes, Human, 16-18*
  • Female
  • Haptoglobins / genetics*
  • Heterozygote
  • Humans

Substances

  • Haptoglobins