Mutation of FGFR3 in a Patient with Craniosynostosis, Hypochondroplasia and Growth Hormone Deficiency

Articles in the same Issue

1. CONTENTS
2. Letter from the Editor
3. Obituary - Dr. Jean Pierre Luton (1933-2002)
4. Role of the Transcription Factor CREB (cAMP Response Element Binding Protein) in Endocrine Tissue Development and Tumorigenesis
5. The Genetics of Autoimmune Thyroid Disease
6. A Novel Insertional Mutation in the Mu-Opioid Receptor Gene is Associated with Altered Cortisol Response to Naloxone
7. Mutations in the TTF2 Gene are Not a Common Finding in Patients with Isolated Cleft Palate and Choanal Atresia
8. 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
9. Mutation of FGFR3 in a Patient with Craniosynostosis, Hypochondroplasia and Growth Hormone Deficiency
10. Clinical, Genetic and Endocrine Aspects of a Patient with 45,X/48,XYYY Mosaicism: Patient Report and Review of the Literature
11. No Evidence for a Role of Genomic Variants in CIT1 in the Etiology of Silver-Russell Syndrome
12. BOOK REVIEWS. CALENDAR. INDEX