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FORUM AND CORRESPONDENCE. BOOK REVIEWS. CALENDAR
Veröffentlicht/Copyright:
1. April 1999
Published Online: 1999-04
©2011 by Walter de Gruyter GmbH & Co.
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Artikel in diesem Heft
- CONTENTS
- Letter from the Editors
- Glucocorticoid Receptor Isoforms Alpha and Beta: Potential Physiological and Pathological Importance
- NeuroD/Beta2 Polymorphism is Not Associated with Type 1 Diabetes in Chinese, Korean, or Caucasian Populations
- CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient
- Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes
- A Novel Mutation (W718S) in the Steroid-Binding Domain of the Androgen Receptor Gene in a Boy with Ambiguous Genitalia and Hypergonadotrophic Hypogonadism
- Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene
- Homozygous Transthyretin Leu64: A Very Rare Transthyretin Mutation Associated With Amyloidosis but Not With Euthyroid Hyperthyroxinemia
- FORUM AND CORRESPONDENCE. BOOK REVIEWS. CALENDAR
Artikel in diesem Heft
- CONTENTS
- Letter from the Editors
- Glucocorticoid Receptor Isoforms Alpha and Beta: Potential Physiological and Pathological Importance
- NeuroD/Beta2 Polymorphism is Not Associated with Type 1 Diabetes in Chinese, Korean, or Caucasian Populations
- CYP11B1 Intragenic Polymorphisms Give Evidence for a Different Q356X Allele in an African-Brazilian Patient
- Mutations in the CFTR Gene are Not a Common Finding in Patients with Diabetes
- A Novel Mutation (W718S) in the Steroid-Binding Domain of the Androgen Receptor Gene in a Boy with Ambiguous Genitalia and Hypergonadotrophic Hypogonadism
- Growth Hormone Insensitivity (Laron Syndrome) in a Russian Girl of Slavic Origin Caused by a Common Mutation of the GH Receptor Gene
- Homozygous Transthyretin Leu64: A Very Rare Transthyretin Mutation Associated With Amyloidosis but Not With Euthyroid Hyperthyroxinemia
- FORUM AND CORRESPONDENCE. BOOK REVIEWS. CALENDAR
