Chromosomal breakage in multiple endocrine adenomatosis (types I and II).

Abstract

Chromosomal analyses of cultured lymphocytes from nine patients with familial multiple endocrine adenomatosis (MEA) syndrome type I from six families and two 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. 

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Cite this paper

@article{Gustavson1983ChromosomalBI, title={Chromosomal breakage in multiple endocrine adenomatosis (types I and II).}, author={Karl H. Gustavson and R. Jansson and Kjell Oberg}, journal={Clinical genetics}, year={1983}, volume={23 2}, pages={143-9} }