Patients with thalassemia develop osteoporosis, osteomalacia, and hypoparathyroidism, all of which are corrected by transfusion.

R. A. Christenson, P. Pootrakul, J. M. Burnell, E. J. Teubner, C. A. Finch, D. J. Baylink

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)409-416
Number of pages8
JournalBirth Defects: Original Article Series
Volume23
Issue number5 A
StatePublished - 1987

ASJC Scopus Subject Areas

  • Developmental Biology
  • Genetics(clinical)

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