Genome Sequencing Explores Complexity of Chromosomal Abnormalities in Recurrent Miscarriage

Recurrent miscarriage (RM) affects millions of couples globally, and half of them have no demonstrated etiology. Genome sequencing (GS) is an enhanced and novel cytogenetic tool to define the contribution of chromosomal abnormalities in human diseases. In this study we evaluated its utility in RM-af...

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Publicado no:Am J Hum Genet
Main Authors: Dong, Zirui, Yan, Junhao, Xu, Fengping, Yuan, Jianying, Jiang, Hui, Wang, Huilin, Chen, Haixiao, Zhang, Lei, Ye, Lingfei, Xu, Jinjin, Shi, Yuhua, Yang, Zhenjun, Cao, Ye, Chen, Lingyun, Li, Qiaoling, Zhao, Xia, Li, Jiguang, Chen, Ao, Zhang, Wenwei, Wong, Hoi Gin, Qin, Yingying, Zhao, Han, Chen, Yuan, Li, Pei, Ma, Tao, Wang, Wen-Jing, Kwok, Yvonne K., Jiang, Yuan, Pursley, Amber N., Chung, Jacqueline P.W., Hong, Yan, Kristiansen, Karsten, Yang, Huanming, Piña-Aguilar, Raul E., Leung, Tak Yeung, Cheung, Sau Wai, Morton, Cynthia C., Choy, Kwong Wai, Chen, Zi-Jiang
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2019
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6904795/
https://ncbi.nlm.nih.gov/pubmed/31679651
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2019.10.003
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