The human embryonic genome is karyotypically complex, with chromosomally abnormal cells preferentially located away from the developing fetus

人类胚胎基因组的核型复杂,染色体异常的细胞优先位于远离发育中的胎儿的位置

阅读:5
作者:D K Griffin, P R Brezina, K Tobler, Yulian Zhao, G Silvestri, R C Mccoy, R Anchan, A Benner, G R Cutting, W G Kearns

Methods

All patients (144 couples) were undergoing routine preimplantation genetic testing for aneuploidy in three IVF clinical settings. Cleavage-stage biopsy preceded chromosome analysis by next-generation sequencing. All patients provided informed consent. Additional molecular testing was carried out on blastocyst embryos and was analyzed for up to four embryonic structures (ICM, TE, Bc and PC). Main

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。