A rare de novo duplication of chromosome 21q22.12 → q22.3 with other concomitant deletion and duplication of small fragments in 21q associated with Down syndrome: Prenatal diagnosi...

por Qi, Qingwei, Zhou, Xiya, Jiang, Yulin, Hao, Na, Zhou, Jing, Zhang, Liang
Publicado 2013

Trisomy 22 with long spina bifida occulta: A case report

por Ma, Li, Ouyang, Yunshu, Qi, Qingwei, Hao, Na, Zhao, Dachun, Jiang, Yuxin, Meng, Hua
Publicado 2018

Prenatal genetic diagnosis of disseminated infantile myofibromatosis: a case report and literature review

por Lü, Yan, Jiang, Yulin, Wu, Huanwen, Qi, Qingwei, Zhou, Xiya, Guo, Qi, Hao, Na, Liu, Juntao, Meng, Hua
Publicado 2023

A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples

por Zhou, Xiya, Chen, Xiangbin, Jiang, Yulin, Qi, Qingwei, Hao, Na, Liu, Chengkun, Xu, Mengnan, Cram, David S., Liu, Juntao
Publicado 2021

Detection of Mosaic Absence of Heterozygosity (AOH) Using Low-Pass Whole Genome Sequencing in Prenatal Diagnosis: A Preliminary Report

por Lü, Yan, Jiang, Yulin, Zhou, Xiya, Hao, Na, Xu, Chenlu, Guo, Ruidong, Chang, Jiazhen, Li, Mengmeng, Zhang, Hanzhe, Zhou, Jing, Zhang, Wei (Victor), Qi, Qingwei
Publicado 2023

Simultaneous Detection of CNVs and SNVs Improves the Diagnostic Yield of Fetuses with Ultrasound Anomalies and Normal Karyotypes

por Qi, Qingwei, Jiang, Yulin, Zhou, Xiya, Meng, Hua, Hao, Na, Chang, Jiazhen, Bai, Junjie, Wang, Chunli, Wang, Mingming, Guo, Jiangshan, Ouyang, Yunshu, Xu, Zhonghui, Xiao, Mengsu, Zhang, Victor Wei, Liu, Juntao
Publicado 2020

Evaluation and Analysis of Absence of Homozygosity (AOH) Using Chromosome Analysis by Medium Coverage Whole Genome Sequencing (CMA-seq) in Prenatal Diagnosis

por Lü, Yan, Jiang, Yulin, Zhou, Xiya, Hao, Na, Lü, Guizhen, Guo, Xiangxue, Guo, Ruidong, Liu, Wenjie, Xu, Chenlu, Chang, Jiazhen, Li, Mengmeng, Zhang, Hanzhe, Zhou, Jing, Zhang, Wei (Victor), Qi, Qingwei
Publicado 2023

Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies

por Chen, Xinlin, Jiang, Yulin, Chen, Ruiguo, Qi, Qingwei, Zhang, Xiujuan, Zhao, Sheng, Liu, Chaoshi, Wang, Weiyun, Li, Yuezhen, Sun, Guoqiang, Song, Jieping, Huang, Hui, Cheng, Chen, Zhang, Jianguang, Cheng, Longxian, Liu, Juntao
Publicado 2022

Ex utero intrapartum therapy in infants with congenital diaphragmatic hernia: a propensity score matching analysis

por Zhao, Yunlong, Wang, Ying, Liu, Chao, Jiang, Yulin, Wei, Yandong, Meng, Hua, Jian, Shan, Zhu, Xiting, Pei, Lijian, Bai, Xiaochen, Feng, Feng, Lv, Yan, Zhou, Xiya, Qi, Qingwei, Li, Jingna, Ma, Lishuang
Publicado 2022