Human alpha-thalassemia syndromes: detection of molecular defects

Am J Hematol. 1996 Oct;53(2):81-91. doi: 10.1002/(SICI)1096-8652(199610)53:2<81::AID-AJH5>3.0.CO;2-#.
No abstract available

Publication types

  • Review

MeSH terms

  • Blotting, Southern
  • Chromosome Mapping
  • Gene Deletion
  • Humans
  • Oligonucleotide Probes
  • Syndrome
  • alpha-Thalassemia / genetics*

Substances

  • Oligonucleotide Probes