Tharapel A T, Wilroy R S, Martens P R, Holbert J M, Summitt R L
Ann Genet. 1983;26(4):229-33.
Two unrelated infants with multiple anomalies and diploid-triploid mosaicism are reported. A comparison of their clinical features with those of twelve published reports with 2n/3n karyotype is provided. The data reveal that 2n/3n mosaicism is a clinically recognizable syndrome.
报道了两名患有多种异常和二倍体 - 三倍体嵌合体的无亲缘关系的婴儿。将他们的临床特征与十二篇已发表的具有2n/3n核型报告中的特征进行了比较。数据显示,2n/3n嵌合体是一种临床上可识别的综合征。