Y. Chu

发表

METTL3-Mediated N6-Methyladenosine Modification Is Involved in the Dysregulation of NRIP1 Expression in Down Syndrome

Fan Yang, B. Hao, S. Liao, 2021, Frontiers in Cell and Developmental Biology.

Experimental endometriosis reduction in rats treated with pioglitazone

Dongyun Zhang, M. He, Hong-yan Liu, 2012 .

The use of cffDNA in fetal sex determination during the first trimester of pregnancy of female DMD carriers.

Dong Wu, S. Liao, Tao Li, 2012, Intractable & rare diseases research.

A novel c.2326G>A KIT pathogenic variant in piebaldism.

B. Hao, S. Liao, Ke Yang, 2020, American journal of translational research.

[Maternal cell contamination of prenatal samples and the potential effects on prenatal diagnosis results].

Zhao‐Yang Zhang, S. Liao, Tao Li, 2013, Zhonghua fu chan ke za zhi.

22q11.2 Deletion Syndrome: Copy Number Variation Analysis in Two Patients

Dong Wu, S. Liao, Y. Chu, 2016 .

DNA methylation study of fetus genome through a genome-wide analysis

M. He, Hongdan Wang, B. Zhu, 2014, BMC Medical Genomics.

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

Hongdan Wang, Dong Wu, S. Liao, 2016, Journal of Biomedical Science.

Mutations in the RS1 gene in a Chinese family with X-linked juvenile retinoschisis.

Dong Wu, S. Liao, Y. Chu, 2012, Intractable & rare diseases research.

Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis.

Dong Wu, S. Liao, Y. Chu, 2016, Taiwanese journal of obstetrics & gynecology.

Integrated miRNA and mRNA expression profiling in fetal hippocampus with Down syndrome

Hongdan Wang, Dong Wu, S. Liao, 2016, Journal of Biomedical Science.