摘要
本文报告作者运用荧光标记的6号、9号、13号、15号、和Y染色体探针,对12名患者的G显带外周血、骨髓或胎儿羊水细胞染色体标本进行染色体原位抑制杂交的研究。
A study of chromosome 6,9,13,15 and Y specific library probes to identify the chromosome abnormalities was reported,The marker chromosome which derived from the chromosome 15,the chromosome translocation of t(2.9), and the very few mosaic 47,XXY cell line in 46,XX cell were exactly identified respectively in patients.
出处
《云南医药》
CAS
1996年第2期120-121,共2页
Medicine and Pharmacy of Yunnan
基金
云南省应用基础研究基金