Novel TSHβ Subunit Gene Mutation Causing Congenital Central Hypothyroidism in a Newborn Male

Articles in the same Issue

1. TABLE OF CONTENTS
2. Communicating with Parents with Full Disclosure: A Case of Cloacal Extrophy with Genital Ambiguity
3. The Use of a Continuous Glucose Monitoring System in Hypoglycemic Disorders
4. Seasonality of Month of Birth among African American Children with Diabetes Mellitus in the City of Chicago
5. HLA-DQA1 and -DQB1 Alleles in Latino and African American Children with Diabetes Mellitus
6. Efficacy of Orlistat as an Adjunct to Behavioral Treatment in Overweight African American and Caucasian Adolescents with Obesity-related Co-morbid Conditions
7. Protease Inhibitor Therapy Improves Protein Catabolism in Prepubertal Children with HIV Infection
8. Homocysteine in a Multi-ethnic Sample of School-age Children
9. The MACIS Score Predicts the Clinical Course of Papillary Thyroid Carcinoma in Children and Adolescents
10. Catch-up Growth in Severe Juvenile Hypothyroidism: Treatment with a GnRH Analog
11. Novel TSHβ Subunit Gene Mutation Causing Congenital Central Hypothyroidism in a Newborn Male
12. Diabetic Ketoacidosis Secondary to Growth Hormone Treatment in a Boy with Prader-Willi Syndrome and Steatohepatitis
13. McCune-Albright Syndrome Associated with Pituitary Microadenoma: Patient Report
14. Classical Phenotype of Laron Syndrome in a Girl with a Heterozygous Mutation and Heterozygous Polymorphism of the Growth Hormone Receptor Gene
15. The First Meeting of the Loop Club
16. CALENDAR