Chromosomal breakage in multiple endocrine adenomatosis (types I and II)
- 1 February 1983
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 23 (2) , 143-149
- https://doi.org/10.1111/j.1399-0004.1983.tb01863.x
Abstract
Chromosomal analyses of cultured lymphocytes from 9 patients with familial multiple endocrine adenomatosis (MEA) syndrome type I from 6 families and 2 patients, father and daughter, with familial MEA syndrome type II showed an increased frequency of chromosomal breakage. The frequency of sister chromatid exchanges was not increased.Keywords
This publication has 5 references indexed in Scilit:
- Chromosome instability in patients with medullary carcinoma of the thyroidJAMA, 1981
- New staining method for the detection of sister-chromatid exchanges in brdu-labelled chromosomesJournal of Cell Science, 1978
- High Resolution of Human ChromosomesScience, 1976
- Differential binding of alkylating fluorochromes in human chromosomesExperimental Cell Research, 1970