CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient

Articles in the same Issue

1. CONTENTS
2. Letter from the Editors
3. Glucocorticoid Receptor Isoforms Alpha and Beta: Potential Physiological and Pathological Importance
4. NeuroD/Beta2 Polymorphism is Not Associated with Type 1 Diabetes in Chinese, Korean, or Caucasian Populations
5. CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient
6. Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes
7. A Novel Mutation (W718S) in the Steroid-Binding Domain of the Androgen Receptor Gene in a Boy with Ambiguous Genitalia and Hypergonadotrophic Hypogonadism
8. Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene
9. Homozygous Transthyretin Leu64: A Very Rare Transthyretin Mutation Associated With Amyloidosis but Not With Euthyroid Hyperthyroxinemia
10. FORUM AND CORRESPONDENCE. BOOK REVIEWS. CALENDAR