Short stature in homozygous β-thalassaemia is due to disproportionate truncal shortening
Author:
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2265.1995.tb02684.x/fullpdf
Reference22 articles.
1. Hypogonadism in β-thalassemic adolescents: A characteristic pituitary-gonadal impairment. The ineffectiveness of long-term iron chelation therapy
2. Growth and sexual maturation in thalassemia major
3. Endocrine involvement in children with β-thalassaemia major. Transverse and longitudinal studies. I. Pituitary-thyroidal axis function and its correlation with serum ferritin levels
4. Prospective study of the hypothalamic-pituitary axis in thalassaemic patients who developed secondary amenorrhoea
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