PMID: 6132690Feb 1, 1983

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

Clinical Genetics
K H GustavsonK Oberg


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.


Mar 26, 1976·Science·J J Yunis
Jun 1, 1970·Experimental Cell Research·T CasperssonC Johansson


Oct 1, 1992·The British Journal of Psychiatry : the Journal of Mental Science·G AknerL Wetterberg
Dec 1, 1988·Journal of Medical Genetics·N E Simpson
Apr 1, 1988·The British Journal of Psychiatry : the Journal of Mental Science·L WetterbergE Håkansson
Aug 1, 1984·World Journal of Surgery·N A SamaanR C Hickey
Jul 1, 1987·American Journal of Medical Genetics·V R BabuC E Jackson
Dec 11, 2008·Cancer Science·Toshihiko TsukadaNaganari Ohkura

Related Concepts

Autosome Abnormalities
Lymphoid Cells
Multiple Endocrine Neoplasia
Genealogical Tree

Related Feeds

Autoimmune Polyendocrine Syndromes

This feed focuses on a rare genetic condition called Autoimmune Polyendocrine Syndromes, which are characterized by autoantibodies against multiple endocrine organs. This can lead to Type I Diabetes.