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Letter from the Editor
Veröffentlicht/Copyright:
1. Oktober 2003
Published Online: 2003-10
©2011 by Walter de Gruyter GmbH & Co.
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Artikel in diesem Heft
- CONTENTS
- Letter from the Editor
- Obituary - Dr. Jean Pierre Luton (1933-2002)
- Role of the Transcription Factor CREB (cAMP Response Element Binding Protein) in Endocrine Tissue Development and Tumorigenesis
- The Genetics of Autoimmune Thyroid Disease
- A Novel Insertional Mutation in the Mu-Opioid Receptor Gene is Associated with Altered Cortisol Response to Naloxone
- Mutations in the TTF2 Gene are Not a Common Finding in Patients with Isolated Cleft Palate and Choanal Atresia
- Effect of Exogenous Insulin-like Growth Factor-I (IGF-I) on the Expression of the IGF-I Gene and the Genes of IGF-Binding Proteins (IGFBPs) 1-4 in Human Thyroid Cells from Nodular Goiter, Follicular Adenoma and Follicular Carcinoma Cultured in Monolayers
- Mutation of FGFR3 in a Patient with Craniosynostosis, Hypochondroplasia and Growth Hormone Deficiency
- Clinical, Genetic and Endocrine Aspects of a Patient with 45,X/48,XYYY Mosaicism: Patient Report and Review of the Literature
- No Evidence for a Role of Genomic Variants in CIT1 in the Etiology of Silver-Russell Syndrome
- BOOK REVIEWS. CALENDAR. INDEX
Artikel in diesem Heft
- CONTENTS
- Letter from the Editor
- Obituary - Dr. Jean Pierre Luton (1933-2002)
- Role of the Transcription Factor CREB (cAMP Response Element Binding Protein) in Endocrine Tissue Development and Tumorigenesis
- The Genetics of Autoimmune Thyroid Disease
- A Novel Insertional Mutation in the Mu-Opioid Receptor Gene is Associated with Altered Cortisol Response to Naloxone
- Mutations in the TTF2 Gene are Not a Common Finding in Patients with Isolated Cleft Palate and Choanal Atresia
- Effect of Exogenous Insulin-like Growth Factor-I (IGF-I) on the Expression of the IGF-I Gene and the Genes of IGF-Binding Proteins (IGFBPs) 1-4 in Human Thyroid Cells from Nodular Goiter, Follicular Adenoma and Follicular Carcinoma Cultured in Monolayers
- Mutation of FGFR3 in a Patient with Craniosynostosis, Hypochondroplasia and Growth Hormone Deficiency
- Clinical, Genetic and Endocrine Aspects of a Patient with 45,X/48,XYYY Mosaicism: Patient Report and Review of the Literature
- No Evidence for a Role of Genomic Variants in CIT1 in the Etiology of Silver-Russell Syndrome
- BOOK REVIEWS. CALENDAR. INDEX
