Genome-wide uniparental disomy screen in human discarded morphologically abnormal embryos

Uniparental disomy (UPD) has been shown to be rare in human normal blastocysts, but its frequency in discarded morphologically abnormal embryos and its relevance to embryonic self-correction of aneuploid remains unknown. The aim of this study was to detect UPD in discarded morphologically abnormal e...

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Detalles Bibliográficos
Autores principales: Xu, Jiawei, Zhang, Meixiang, Niu, Wenbin, Yao, Guidong, Sun, Bo, Bao, Xiao, Wang, Linlin, Du, Linqing, Sun, Yingpu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508668/
https://www.ncbi.nlm.nih.gov/pubmed/26194013
http://dx.doi.org/10.1038/srep12302

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4508668/
https://www.ncbi.nlm.nih.gov/pubmed/26194013
http://dx.doi.org/10.1038/srep12302

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