True Hermaphroditism in an XY Individual due to a Familial Point Mutation of the SRY Gene

Articles in the same Issue

1. TABLE OF CONTENTS
2. Congenital Malformations and Developmental Changes of the Breast: A Neonatological View
3. Pediatric Endocrine Diseases in Pre-Hispanic Aztecs
4. Clustering of Cases of Type 1 Diabetes Mellitus Occurring 2-4 Years After Vaccination is Consistent with Clustering After Infections and Progression to Type I Diabetes Mellitus in Autoantibody Positive Individuals
5. Effects of Insulin-like Growth Factor-I Deficiency and Replacement Therapy on the Hematopoietic System in Patients with Laron Syndrome (Primary Growth Hormone Insensitivity)
6. Thyroid Hormone Synthesis and Storage in the Thyroid Gland of Human Neonates
7. Bisphosphonates, a New Treatment for Glucocorticoid-induced Osteoporosis in Children
8. Measured Length of Normal Term Infants Changes Over the First Two Days of Life
9. Validity of the Use of a Few Hand-Wrist Bones for Assessing Bone Age
10. Dissatisfaction with Height and Weight, and Attempts at Height Gain and Weight Control in Korean School-Children
11. Insulin Resistance and Hyperinsulinemia in Prepubertal Obese Children
12. Testicular Descent Related to Growth Hormone Treatment
13. Monozygotic Twins with Congenital Adrenal Hyperplasia: Long-term Endocrine Evaluation and Gene Analysis
14. Adult Type Granulosa Cell Tumor Causing Precocious Pseudopuberty in a 6 Year-old Girl
15. True Hermaphroditism in an XY Individual due to a Familial Point Mutation of the SRY Gene
16. BOOK REVIEWS. CALENDAR