Jieping Song

发表

Non-invasive Prenatal Diagnosis of Chromosomal Aneuploidies and Microdeletion Syndrome Using Fetal Nucleated Red Blood Cells Isolated by Nanostructure Microchips

Xingzhong Zhao, Xuechen B Yu, Yuan-zhen Zhang, 2018, Theranostics.

Two de novo Overlapping Interstitial Duplications at 10q22 Associated with Speech Impairments, Behaviour Problems, Genital Anomalies, Developmental Delay and Intellectual Disability

Haiming Yuan, Weipeng Wang, Hui Li, 2017 .

Genetic deconvolution of fetal and maternal cell-free DNA in maternal plasma enables next-generation non-invasive prenatal screening

Xiaoqiang Cai, Congjian Xu, Xiaotian Li, 2022, Cell Discovery.

A feasibility study of noninvasive prenatal diagnosis in facioscapulohumeral muscular dystrophy type 1 in a Chinese family

Bo Wang, Yiming Wu, Hui Li, 2022, Frontiers in Genetics.

Clinical and genetic study of three families with 15q11q13 duplications.

Bo Wang, Jieping Song, Xu Liu, 2022, Taiwanese journal of obstetrics & gynecology.

Prenatal diagnosis and genetic counseling of a 10p11.23q11.21 duplication associated with normal phenotype

Bo Wang, Cheng-rong Zhang, Wei Jiang, 2022, Molecular cytogenetics.

The prevalence and outcomes of α- and β-thalassemia among pregnant women in Hubei Province, Central China

Miaomiao Chen, Yao Cheng, Guoqiang Sun, 2022, Medicine.

Decidual vascular endothelial cells promote maternal–fetal immune tolerance by inducing regulatory T cells through canonical Notch1 signaling

Weipeng Wang, Jieping Song, Yan-yi Yao, 2016, Immunology and cell biology.

A family with Robertsonian translocation: a potential mechanism of speciation in humans

Xi Li, Bo Wang, Han Rong, 2016, Molecular Cytogenetics.

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

Guoqiang Sun, Juntao Liu, Xinlin Chen, 2022, Journal of translational medicine.

Genome sequencing combining prenatal ultrasound in the evaluation of fetal CNS structural anomalies

Xun Xu, Shida Zhu, Z. Yin, 2020 .

Perinatal outcomes of prenatal cases testing positive for trisomy 9 by noninvasive prenatal testing.

Wei Wang, Jieping Song, Yan-yi Yao, 2022, Taiwanese journal of obstetrics & gynecology.

Identification of a novel 10.3 kb deletion causing α0-thalassemia by the third-generation sequencing: pedigree analysis and genetic diagnosis.

Jiaqi Li, Hui Li, Yayun Qin, 2023, Clinical biochemistry.

A rare case of uniparental isodisomy of chromosome 19 with no phenotypic abnormalities.

Bo Wang, Jieping Song, Ting Zhou, 2021, Taiwanese Journal of Obstetrics & Gynecology.

Analysis of meiotic segregation patterns and interchromosomal effects insperm from a Robertsonian translocation family

Bo Wang, K. Fang, Weipeng Wang, 2014 .

Case Report: Potential Speciation in Humans Involving RobertsonianTranslocations.

Bo Wang, Weipeng Wang, Yanping Tang, 2013 .

Two Novel Mutations in the C-Terminal Region of Centrosomal Protein 290 (CEP290) Result in Classic Joubert Syndrome

Shuang Yang, F. Mu, Lixia Wang, 2015, Journal of child neurology.