A Family with Isolated Hyperparathyroidism Segregating a Missense MEN1 Mutation and Showing Loss of the Wild-Type Alleles in the Parathyroid Tumors
- 1 November 1998
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 63 (5) , 1544-1549
- https://doi.org/10.1086/302097
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Characterization of Mutations in Patients with Multiple Endocrine Neoplasia Type 1American Journal of Human Genetics, 1998
- Recent advances in multiple endocrine neoplasia type ICurrent Opinion in Endocrinology, Diabetes and Obesity, 1998
- Somatic mutation of the MEN1 gene in parathyroid tumoursNature Genetics, 1997
- Familial Hyperparathyroidism without Multiple Endocrine NeoplasiaWorld Journal of Surgery, 1997
- Sporadic Primary Hyperparathyroidism in the Setting of Multiple Endocrine Neoplasia Type 1Archives of Surgery, 1996
- TheRETProto-Oncogene in Multiple Endocrine Neoplasia Type 2 and Hirschsprung's DiseaseNew England Journal of Medicine, 1996
- A Program Using Loss-of-Constitutional-Heterozygosity Data to Ascertain the Location of Predisposing Genes in Cancer FamiliesHuman Heredity, 1995
- Familial isolated primary hyperparathyroidismClinical Endocrinology, 1994
- Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinomaNature, 1988