Jie Li

发表

Identification of copy number variations associated with congenital heart disease by chromosomal microarray analysis and next‐generation sequencing

D. Cram, Yali Hu, Yingsong Yang, 2016, Prenatal diagnosis.

Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series.

Xing Wu, Wei Liu, Yingsong Yang, 2021, Taiwanese journal of obstetrics & gynecology.

A case of an infertile male with a small supernumerary marker chromosome negative for M-FISH and containing only heterochromatin

Yali Hu, Yaping Wang, Wei Wang, 2009, Journal of Assisted Reproduction and Genetics.

The application of chromosomal microarray analysis to the prenatal diagnosis of isolated mild ventriculomegaly.

Guangfeng Zhao, Xiang-yu Zhu, Jie Li, 2019, Taiwanese journal of obstetrics & gynecology.

A novo missense variant of the PHEX gene in patients with X-linked dominant hypophosphatemia

Wei Liu, Xiang-yu Zhu, Jie Li, 2020 .

Lymphocyte subpopulations in Chinese women with Turner syndrome

Yali Hu, H. Fan, Yayi Hou, 2012, Archives of Gynecology and Obstetrics.

Application of chromosomal microarray analysis in products of miscarriage

Xing Wu, Yali Hu, Yuanyuan Gu, 2018, Molecular Cytogenetics.

Cell-free DNA test for pathogenic copy number variations: A retrospective study.

D. Cram, Wei Liu, Yali Hu, 2021, Taiwanese journal of obstetrics & gynecology.

[Prenatal diagnosis and follow-up of a case with Lowe syndrome caused by interstitial deletion of Xq25-26].

Yali Hu, T. Ru, Xiang-yu Zhu, 2017, Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics.

Application of chromosomal microarray analysis in products of miscarriage

Xing Zheng Wu, Yali Hu, Yuanyuan Gu, 2018, Molecular Cytogenetics.

Fetal congenital gastrointestinal obstruction: prenatal diagnosis of chromosome microarray analysis and pregnancy outcomes

Xing Wu, Wei Liu, Yan Xu, 2023, BMC Pregnancy and Childbirth.

Long-read sequencing: An effective method for genetic analysis of CYP21A2 variation in congenital adrenal hyperplasia.

Aiping Mao, Jiaqi Li, Shilai Bao, 2023, Clinica chimica acta; international journal of clinical chemistry.

Maternal Serum PLGF, PAPPA, β-hCG and AFP Levels in Early Second Trimester as Predictors of Preeclampsia.

Guangfeng Zhao, Biyun Xu, Jie Li, 2017, Clinical laboratory.