染色体原位抑制杂交鉴别染色体易位的研究

Research of chromosme translocation and marker chromosome using chromosome in situ suppression hybridization

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.