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Clin Genet. 1983 Feb;23(2):143-9.

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.

PMID:
6132690
[Indexed for MEDLINE]
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