Genetic and clinical characterization of sporadic cystic parathyroid tumours
- 1 February 2002
- journal article
- research article
- Published by Wiley in Clinical Endocrinology
- Vol. 56 (2), 261-269
- https://doi.org/10.1046/j.0300-0664.2001.01469.x
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- Homozygous inactivation of the MEN1 gene as a specific somatic event in a case of secondary hyperparathyroidismActa Endocrinologica, 2001
- Loss of heterozygosity in sporadic parathyroid tumours: involvement of chromosome 1 and the MEN1 gene locus in 11q13.Clinical Endocrinology, 2000
- A 6-Mb High-Resolution Physical and Transcription Map Encompassing the Hereditary Prostate Cancer 1 (HPC1) RegionGenomics, 2000
- Immunohistochemical Detection of Somatostatin Receptor Subtypes sst1 and sst2A in Human Somatostatin Receptor Positive TumorsJournal of Clinical Endocrinology & Metabolism, 1999
- Comparative Genomic Hybridization Analysis of Human Parathyroid TumorsCancer Genetics and Cytogenetics, 1998
- Positional Cloning of the Gene for Multiple Endocrine Neoplasia-Type 1Science, 1997
- Differential loss of heterozygosity in familial, sporadic, and uremic hyperparathyroidismHuman Genetics, 1997
- Frequent loss of chromosome arm Ip DNA in parathyroid adenomasGenes, Chromosomes and Cancer, 1995
- Monoclonality and Abnormal Parathyroid Hormone Genes in Parathyroid AdenomasNew England Journal of Medicine, 1988
- Fat staining in parathyroid disease—Diagnostic value and impact on surgical strategy: Clinicopathologic analysis of 191 casesHuman Pathology, 1985