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Ying Peng

6PUBLICATIONS

7CO-AUTHORS

Gene mappingFoetal development and medicineEpigenetics (incl. genome methylation and epigenomics)

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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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Frequent Collaborators

2 joint publications

Zhuo Li

2 joint publications

Na Ma

2 joint publications

Hui Xi

1 joint publications

Lingqian Wu

1 joint publications

Juan Du

1 joint publications

Wanqin Xie

1 joint publications

Ranhui Duan

Frequent Collaborators

2 joint publications

Zhuo Li

2 joint publications

Na Ma

2 joint publications

Hui Xi

1 joint publications

Lingqian Wu

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