Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature

Articles in the same Issue

1. CONTENTS
2. Letter from the Editors
3. The Human Genome Project, Positional Cloning of Inherited Disease Genes, and Multiple Endocrine Neoplasia Type 1
4. The "Little People" of the Island of Krk - Revisited. Etiology of Hypopituitarism Revealed
5. Further Delineation of Spondyloepimetaphyseal Dysplasia Shohat Type, and a Review of the Literature
6. Genetic Analyses of a Family with Familial Medullary and Papillary Thyroid Carcinoma
7. Neuromas in Multiple Endocrine Neoplasia Type 2A with a RET Codon 611 Mutation
8. Germline V804M Mutation in the RET Proto-oncogene in Two Apparently Sporadic Cases of MTC Presenting in the Seventh Decade of Life
9. Thyroid Abnormalities in Peutz-Jeghers Syndrome: Report of a New Observation and Review of the Literature
10. Non-Classical Congenital Adrenal Hyperplasia Phenotype in a Female Newborn Heterozygous for the 21-Hydroxylase Gene Mutation
11. BOOK REVIEWS. CALENDAR