Cytogenetic studies of individuals from four kindreds with multiple endocrine neoplasia type II syndrome
- 1 October 1987
- journal article
- research article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 28 (2) , 253-260
- https://doi.org/10.1016/0165-4608(87)90211-1
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- High resolution chromosome and DNA analysis in multiple endocrine neoplasia type II syndromeCancer Genetics and Cytogenetics, 1987
- Absence of chromosomal instability in one kindred with multiple endocrine neoplasia type 2ACancer Genetics and Cytogenetics, 1986
- LINKAGE ANALYSIS OF A DNA MARKER LOCALIZED TO 20P12 AND MULTIPLE ENDOCRINE NEOPLASIA TYPE-2A1985
- Chromosomal instability in medullary carcinoma of the thyroidWorld Journal of Surgery, 1984
- Chromosome 20 deletion in human multiple endocrine neoplasia types 2A and 2B: a double-blind study.Proceedings of the National Academy of Sciences, 1984
- Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred.Journal of Medical Genetics, 1984
- Genetic studies of multiple endocrine neoplasia type 2 syndromes: a workshop commentary.1984
- Linkage and chromosome study of multiple endocrine neoplasia IIaCancer Genetics and Cytogenetics, 1983
- Chromosomal breakage in multiple endocrine adenomatosis (types I and II)Clinical Genetics, 1983
- STUDY OF A KINDRED WITH PHEOCHROMOCYTOMA, MEDULLARY THYROID CARCINOMA, HYPERPARATHYROIDISM AND GUSHING ʼS DISEASE: MULTIPLE ENDOCRINE NEOPLASIA, TYPE 21Medicine, 1968