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Systems Biology in Reproductive Medicine Volume 65, 2019 - Issue 3
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Clinical: Research Communication

Clinical application of NGS-based SNP haplotyping for the preimplantation genetic diagnosis of primary open angle glaucoma

Xingzhe JiAssisted Reproduction Centre, Northwest Women’s and Children’s Hospital, Xi’an, ChinaView further author information
,
Zhou ZhangAssisted Reproduction Centre, Northwest Women’s and Children’s Hospital, Xi’an, ChinaView further author information
,
Juanzi ShiAssisted Reproduction Centre, Northwest Women’s and Children’s Hospital, Xi’an, ChinaView further author information
&
Bin HePrenatal Diagnosis Centre, Northwest Women’s and Children’s Hospital, Xi’an, ChinaCorrespondence[email protected]
View further author information
Pages 258-263 | Received 06 Dec 2018, Accepted 24 Feb 2019, Published online: 12 Apr 2019

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Read on this site (2)

Bin He, Lin Wang, Qiuhua Wu, Xiaobin Wang, Xingzhe Ji, Wenhao Shi, Juanzi Shi, Rong Qiang & Shuai Zhen. (2022) Clinical application of NGS-based SNP haplotyping for PGT-M of methylmalonic acidemia. Systems Biology in Reproductive Medicine 68:1, pages 80-88.
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Dongjia Chen, Xiaoting Shen, Yan Xu, Chenhui Ding, Qingjian Ye, Yiping Zhong, Yanwen Xu & Canquan Zhou. (2021) Successful four-factor preimplantation genetic testing: α- and β-thalassemia, human leukocyte antigen typing, and aneuploidy screening. Systems Biology in Reproductive Medicine 67:2, pages 151-159.
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Articles from other publishers (8)

Dongjia Chen, Yan Xu, Yu Fu, Yali Wang, Yuliang Liu, Chenhui Ding, Bing Cai, Jiafu Pan, Jing Wang, Rong Li, Jing Guo, Han Zhang, Yanhong Zeng, Xiaoting Shen & Canquan Zhou. (2023) Clinical application of next generation sequencing-based haplotype linkage analysis in the preimplantation genetic testing for germline mosaicisms. Orphanet Journal of Rare Diseases 18:1.
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Yujun Liu & Xu Zhi. (2021) Advances in Genetic Diagnosis of Kallmann Syndrome and Genetic Interruption. Reproductive Sciences 29:6, pages 1697-1709.
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Li-Li Lu, Xiao-Juan Hu, Yan Yang, Shen Xu, Shi-Yong Yang, Cui-Yu Zhang & Qing-Ya Zhao. (2022) Correlation of myopia onset and progression with corneal biomechanical parameters in children. World Journal of Clinical Cases 10:5, pages 1548-1556.
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Cuiting Peng, Jun Ren, Yutong Li, Yuezhi Keqie, Fan Zhou, Xuemei Zhang, Hongmei Zhu, Ting Hu, He Wang, Xinlian Chen & Shanling Liu. (2021) Preimplantation Genetic Testing for Rare Inherited Disease of MMA-CblC: an Unaffected Live Birth. Reproductive Sciences 28:12, pages 3571-3578.
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Yao Zhou, Xiaohui Yang, Zheng Liu, Yu Zhang, Huaye Chen, Yongfang Zhang, Yuxin Hu, Yanlin Ma & Qi Li. (2021) Excluding embryos with two novel mutations in FREM2 gene by the next-generation sequencing-based single nucleotide polymorphism haplotyping. Aging 13:22, pages 24786-24794.
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Dongjia Chen, Xiaoting Shen, Yan Xu, Bing Cai, Chenhui Ding, Yiping Zhong, Yanwen Xu & Canquan Zhou. (2021) Next-Generation Sequencing-Based Preimplantation Genetic Testing for De Novo NF1 Mutations. BioChip Journal 15:1, pages 69-76.
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Dongjia Chen, Xiaoting Shen, Changsheng Wu, Yan Xu, Chenhui Ding, Guirong Zhang, Yanwen Xu & Canquan Zhou. (2020) Eleven healthy live births: a result of simultaneous preimplantation genetic testing of α- and β-double thalassemia and aneuploidy screening. Journal of Assisted Reproduction and Genetics 37:3, pages 549-557.
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Haining Luo, Chao Chen, Yun Yang, Yinfeng Zhang, Yuan Yuan, Wanyang Wang, Renhua Wu, Zhiyu Peng, Ying Han, Lu Jiang, Ruqiang Yao, Xiaoying An, Weiwei Zhang, Yanqun Le, Jiale Xiang, Na Yi, Hui Huang, Wei Li, Yunshan Zhang & Jun Sun. (2019) Preimplantation genetic testing for a family with usher syndrome through targeted sequencing and haplotype analysis. BMC Medical Genomics 12:1.
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