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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I publikationen:Am J Hum Genet
Huvudupphovsmän: 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
Materialtyp: Artigo
Språk:Inglês
Publicerad: Elsevier 2019
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Article
Länkar: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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