Mutations of the Steroid 21-Hydroxylase Gene in an Argentinian Population of 36 Patients with Classical Congenital Adrenal Hyperplasia

Articles in the same Issue

1. TABLE OF CONTENTS
2. Letter from the Editors
3. Evaluation of the Clinical Utility of the Ultrasensitive Immunofluorometric Assay for Growth Hormone (GH) and of the Cortisol Secretory Pattern in Prediction of the Linear Growth Response to Treatment with GH
4. Increase in Bone Density and Plasma Osteocalcin During Growth Hormone Therapy in Growth Hormone Deficient Children
5. Growth Hormone-Insulin-Like Growth Factor-I (IGF-I) Axis in Prepubertal Children with Chronic Renal Failure
6. Factors Predictive of Response to Growth Hormone Therapy in Turner's Syndrome
7. Growth Hormone Release by the Novel GH Releasing Peptide Hexarelin in Patients with Homozygous β-Thalassemia
8. Growth Hormone Treatment in Irradiated Children with Brain Tumors
9. Vitamin A and Beta Carotene Levels in Constitutional Delay of Growth and Puberty
10. Mutations of the Steroid 21-Hydroxylase Gene in an Argentinian Population of 36 Patients with Classical Congenital Adrenal Hyperplasia
11. Maturity-Onset Diabetes of the Young (MODY): Three Case Reports and New Perspectives
12. Growth Hormone Deficiency in Autoimmune Polyglandular Syndrome
13. A Case of Isolated Growth Hormone (GH) Deficiency with Compound Heterozygous Abnormality at the GH-I Gene Locus
14. Hashimoto's Thyroiditis and Mixed Connective Tissue Disease in an 11 Year-Old Girl
15. Long-Term Diazoxide Treatment in Persistent Hyperinsulincmic Hypoglycemia of Infancy: A Case Report
16. BOOK REVIEWS