6,XX Maleness and 46,XX 21-Hydroxylase Deficiency in Dizygotic Twins: Association or Coincidence?

Articles in the same Issue

1. TABLE OF CONTENTS
2. EDITORIAL
3. An Update on the Treatment of Precocious Puberty in McCune-Albright Syndrome and Testotoxicosis
4. European Society for Paediatric Endocrinology (ESPE)
5. The Face of Late-onset Congenital Adrenal Hyperplasia
6. Thyroid Autoimmunity in Children and Adolescents with Type 1 Diabetes Mellitus: Prevalence and Risk Factors
7. Neurocognitive Profile in Turner's syndrome is Not Affected by Growth Impairment
8. Predicting the Growth Response to Growth Hormone (GH) Treatment in Prepubertal and Pubertal Children with Isolated GH Deficiency - Model Validation in an Observational Setting (GeNeSIS)
9. The Course of Neonatal Cholestasis in Congenital Combined Pituitary Hormone Deficiency
10. Criteria for Oral Glucose Tolerance Testing of Obese Minority Youth
11. The Effects of Nutritional-Physical Activity School-based Intervention on Fatness and Fitness in Preschool Children
12. Ghrelin - An Indicator for Fat Oxidation in Obese Children and Adolescents During a Weight Reduction Program
13. Resolution of Severe Sinus Vein Thrombosis with Super Selective Thrombolysis in a Preadolescent with Diabetic Ketoacidosis and a Prothrombin Gene Mutation
14. Remission of Congenital Diabetes Insipidus After Eight Years
15. Metabolic Syndrome Manifestations in an Adolescent with Acrodysostosis
16. 6,XX Maleness and 46,XX 21-Hydroxylase Deficiency in Dizygotic Twins: Association or Coincidence?
17. CALENDAR