Orye E, van Bever H
Ann Genet. 1985;28(1):61-2.
A boy is described, who shares many of the clinical features found in the few patients with a partial 17q trisomy known at present. Karyotyping revealed a de novo 17q+ chromosome, interpretable as a tandem duplication of the distal long arm region 17q25.
本文描述了一名男孩，他具有目前已知的少数部分17号染色体三体患者的许多临床特征。染色体核型分析显示一条新发的17q+染色体，可解释为17q25远端长臂区域的串联重复。
