No Evidence for Additional Imprinting Defects in Silver-Russell Syndrome Patients with Maternal Uniparental Disomy 7 or 11p15 Epimutation

Articles in the same Issue

1. TABLE OF CONTENTS
2. EDITORIAL
3. Update on Coeliac Disease and Type 1 Diabetes Mellitus in Childhood
4. McCune-Albright Syndrome
5. Thyroid Function in Extremely Premature Neonates: A Reference Database
6. Thyroid Function in Preterm Infants 27-29 Weeks of Gestational Age During the First Four Months of Life: Results from a Prospective Study Comprising 80 Preterm Infants
7. Adrenal Steroid Concentrations in Children Seven to Seventeen Years of Age
8. Kinetic Profiles of 18 Systemic Pro- and Anti-Inflammatory Mediators During and Following Exercise in Children
9. Administration of Arginine plus Growth Hormone Releasing Hormone to Evaluate Growth Hormone (GH) Secretory Status in Children with GH Deficiency
10. The Effects of Recombinant Human Growth Hormone on Linear Growth in Children with Crohn's Disease and Short Stature
11. Foot Length Before and During Insulin-like Growth Factor-I Treatment of Children with Laron Syndrome Compared to Human Growth Hormone Treatment of Children with Isolated Growth Hormone Deficiency
12. No Evidence for Additional Imprinting Defects in Silver-Russell Syndrome Patients with Maternal Uniparental Disomy 7 or 11p15 Epimutation
13. Precocious Puberty in a Girl with Floating-Harbor Syndrome
14. The Variable Clinical Phenotype of Liver Glycogen Synthase Deficiency
15. CALENDAR. INDEX