Absence of Mutation in the Follicle-Stimulating Hormone Receptor Gene in Severe Primary Hypothyroidism Associated with Gonadal Hyperstanulation

Articles in the same Issue

1. TABLE OF CONTENTS
2. EDITORIAL
3. McCune-Albright Syndrome and Disorders Due to Activating Mutations of GNAS1
4. Complete Penoscrotal Transposition Associated with Aortic Stenosis in a Newborn
5. Growth and Pubertal Characteristics in Patients with Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
6. Androgen Receptor Genotyping in a Large Australasian Cohort with Androgen Insensitivity Syndrom? Identification of Four Novel Mutations
7. Four Novel Mutations, Including the First Gross Deletion in TCF1, identified in HNF4a, GCK and TCF1 in Patients with MODY in Israel
8. Absence of Mutation in the Follicle-Stimulating Hormone Receptor Gene in Severe Primary Hypothyroidism Associated with Gonadal Hyperstanulation
9. Osteoporosis and Multiple Fractures in an Antiretroviral-naive, HIV-Positive Child
10. Development of Pulmonary Hypertension in an Infant Treated with Diazoxide
11. Acromegaly Symptoms Without Pituitary Adenoma in an Adolescent
12. CALENDAR