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

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	409-416
Number of pages	8
Journal	Birth Defects: Original Article Series
Volume	23
Issue number	5 A
State	Published - 1987

ASJC Scopus Subject Areas

@article{2143d0d139fd4bbe8a525119dceb21a6,

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

author = "Christenson, \{R. A.\} and P. Pootrakul and Burnell, \{J. M.\} and Teubner, \{E. J.\} and Finch, \{C. A.\} and Baylink, \{D. J.\}",

year = "1987",

language = "English",

volume = "23",

pages = "409--416",

journal = "Birth Defects: Original Article Series",

issn = "0547-6844",

number = "5 A",

}

TY - JOUR

T1 - Patients with thalassemia develop osteoporosis, osteomalacia, and hypoparathyroidism, all of which are corrected by transfusion.

AU - Christenson, R. A.

AU - Pootrakul, P.

AU - Burnell, J. M.

AU - Teubner, E. J.

AU - Finch, C. A.

AU - Baylink, D. J.

PY - 1987

Y1 - 1987

UR - https://www.scopus.com/pages/publications/0023480699

UR - https://www.scopus.com/pages/publications/0023480699#tab=citedBy

M3 - Article

C2 - 3689925

AN - SCOPUS:0023480699

SN - 0547-6844

VL - 23

SP - 409

EP - 416

JO - Birth Defects: Original Article Series

JF - Birth Defects: Original Article Series

IS - 5 A

ER -