1. A De Novo heterozygous frameshift mutation identified in BCL11B causes neurodevelopmental disorder by whole exome sequencing. Issue 9 (25th July 2019) Authors: Qiao, Fengchang; Wang, Chen; Luo, Chunyu; Wang, Yan; Shao, Binbin; Tan, Jianxin; Hu, Ping; Xu, Zhengfeng Journal: Molecular genetics & genomic medicine Issue: Volume 7:Issue 9(2019) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel LGI1 mutation causing autosomal dominant lateral temporal lobe epilepsy confirmed by a precise knock‐in mouse model. (12th November 2021) Authors: Hu, Ping; Wu, Dan; Zang, Yan‐Yu; Wang, Yan; Zhou, Ya‐Ping; Qiao, Fengchang; Teng, Xiao‐Yu; Chen, Jiang; Li, Qing‐Qing; Sun, Jia‐Hui; Liu, TingTing; Feng, Hao‐Yang; Zhou, Qi‐Gang; Shi, Yun Stone; Xu, Zhengfeng Journal: CNS neuroscience & therapeutics Issue: Volume 28:Number 2(2022) Page Start: 237 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Analysis of chromosome 22q11 copy number variations by multiplex ligation-dependent probe amplification for prenatal diagnosis of congenital heart defect. Issue 1 (December 2015) Authors: Zhang, Jingjing; Ma, Dingyuan; Wang, Yan; Cao, Li; Wu, Yun; Qiao, Fengchang; Liu, An; Li, Li; Lin, Ying; Liu, Gang; Liu, Cuiyun; Hu, Ping; Xu, Zhengfeng Journal: Molecular cytogenetics Issue: Volume 8:Issue 1(2015) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Application of next-generation sequencing for the diagnosis of fetuses with congenital heart defects. Issue 2 (April 2019) Authors: Qiao, Fengchang; Hu, Ping; Xu, Zhengfeng Journal: Current opinion in obstetrics and gynecology Issue: Volume 31:Issue 2(2019:Apr.) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Circular RNA PVT1 expression and its roles in acute lymphoblastic leukemia. (25th April 2018) Authors: Hu, Jiaojiao; Han, Qi; Gu, Yan; Ma, Jinlong; McGrath, Mary; Qiao, Fengchang; Chen, Baoan; Song, Chunhua; Ge, Zheng Journal: Epigenomics Issue: Volume 10:Number 6(2018) Page Start: 723 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore Sequencing. (23rd December 2021) Authors: Wang, Ya; Tan, Jianxin; Wang, Yan; Liu, An; Qiao, Fengchang; Huang, Mingtao; Zhang, Cuiping; Zhou, Jing; Hu, Ping; Xu, Zhengfeng Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Diagnosis of Shashi-Pena Syndrome Caused by Chromosomal Rearrangement Using Nanopore Sequencing. (December 2021) Authors: Wang, Ya; Tan, Jianxin; Wang, Yan; Liu, An; Qiao, Fengchang; Huang, Mingtao; Zhang, Cuiping; Zhou, Jing; Hu, Ping; Xu, Zhengfeng Journal: Neurology Issue: Volume 7:Number 6(2021) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole‐exome sequencing. Issue 11 (11th August 2020) Authors: Zhou, Xiaoyan; Wang, Yan; Shao, Binbin; Wang, Chen; Hu, Ping; Qiao, Fengchang; Xu, Zhengfeng Journal: Journal of clinical laboratory analysis Issue: Volume 34:Issue 11(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Perinatal outcomes following cell‐free DNA screening in >32 000 women: Clinical follow‐up data from a single tertiary center. (27th July 2018) Authors: Liang, Dong; Lin, Ying; Qiao, Fengchang; Li, Hang; Wang, Yan; Zhang, Jingjing; Liu, An; Ji, Xiuqing; Ma, Dingyuan; Jiang, Tao; Hu, Ping; Xu, Zhengfeng Journal: Prenatal diagnosis Issue: Volume 38:Number 10(2018) Page Start: 755 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Proline‐rich transmembrane protein 2 specifically binds to GluA1 but has no effect on AMPA receptor‐mediated synaptic transmission. Issue 2 (8th January 2022) Authors: Feng, Hao‐Yang; Qiao, Fengchang; Tan, Jianxin; Zhang, Xiaozuo; Hu, Ping; Shi, Yun Stone; Xu, Zhengfeng Journal: Journal of clinical laboratory analysis Issue: Volume 36:Issue 2(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗