Ying Peng
6PUBLICATIONS
7CO-AUTHORS
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Publications (6)
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|Jul 22, 2021
Prenatal case of Simpson-Golabi-Behmel syndrome with a de novo 370Kb-sized microdeletion of Xq26.2 compassing partial GPC3 gene and review.Jing Liu, Qin Liu, Shuting Yang
|May 31, 2021
Implementation of fragile X syndrome carrier screening during prenatal diagnosis: A pilot study at a single center.Hui Xi, Wanqin Xie, Jing Chen
|Apr 09, 2021
Clinical and genetic analysis of classical Ehlers-Danlos syndrome patient caused by synonymous mutation in COL5A2.Na Ma, Zhenhua Zhu, Jing Liu
|Jan 20, 2021
Whole genome sequencing reveals translocation breakpoints disrupting TP63 gene underlying split hand/foot malformation in a Chinese family.Ying Peng, Shuting Yang, Hui Xi
|Jun 17, 2020
Identification of a novel gross deletion of TCOF1 in a Chinese prenatal case with Treacher Collins syndrome.Jing Liu, Pengsiyuan Lin, Jialun Pang
|Jun 06, 2020
Clinical and molecular characterization of 12 prenatal cases of Cri-du-chat syndrome.Ying Peng, Jialun Pang, Jiancheng Hu
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