Gustavson K H, Jansson R, Oberg K
Clin Genet. 1983 Feb;23(2):143-9. doi: 10.1111/j.1399-0004.1983.tb01863.x.
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.
对来自六个家族的九名患有I型家族性多发性内分泌腺瘤(MEA)综合征的患者以及两名患有II型家族性MEA综合征的患者(父女)的培养淋巴细胞进行染色体分析,结果显示染色体断裂频率增加。姐妹染色单体交换频率并未增加。