Novel Deletion Mutations of the DAX1 (NR0B1) Gene in Two Taiwanese Families with X-Linked Adrenal Hypoplasia Congenita

Articles in the same Issue

1. TABLE OF CONTENTS
2. Leptin Levels in Boys with Pubertal Gynecomastia
3. Endocrine Disorders Associated with Holoprosencephaly
4. Are Factors at Diagnosis of Growth Hormone Deficiency in Childhood Associated with Persistence of Growth Hormone Deficiency into Adult Life?
5. Response to Growth Hormone with Respect to Pubertal Status on Increased Dose in Idiopathic Growth Hormone Deficiency: An Analysis of Turkish Children in the KIGS Database (Pfizer International Growth Study)
6. Growth Hormone Releasing Hormone Receptor (GHRH-R) Gene Mutation in Indian Children with Familial Isolated Growth Hormone Deficiency: A Study from Western India
7. Body Composition, Dehydroepiandrosterone Sulfate and Leptin Concentrations in Girls Approaching Menarche
8. Valproate-induced Insulin Resistance in Prepubertal Girls with Epilepsy
9. Novel Deletion Mutations of the DAX1 (NR0B1) Gene in Two Taiwanese Families with X-Linked Adrenal Hypoplasia Congenita
10. Comparison of Clinical, Radiological and Molecular Findings in Korean Infants and Children with Achondroplasia and Hypochondroplasia
11. Serum Zinc, Insulin-like Growth Factor-I and Insulin-like Growth Factor Binding Protein-3 Levels in Children with Type 1 Diabetes Mellitus
12. Primary Ovarian Failure and Deletions of the Long Arm of Chromosome 3
13. Hypertrichosis Cubiti (Hairy Elbow Syndrome): A Clue to a Malformation Syndrome
14. Central Precocious Puberty with an Incidental Suprasellar Lipoma
15. CALENDAR