Lingji Chen - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

Lingji Chen

Showing results (11-20 of 36) with videos related to

Pageof 4

Sort By:

Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|August 8, 2021

[Study on clinical features and diagnostic methods of prenatal Wolf-Hirschhorn syndrome]Yan Wang, Xuemei Chen, Huili Xue, et al.

International Journal of Clinical and Experimental Pathology|January 15, 2020

Frequencies and hematological manifestations of the HKαα allele in southern Chinese populationMin Zhang, Hailong Huang, Meihuan Chen, et al.

Medicine|May 20, 2021

Diagnostic accuracy and value of chromosomal microarray analysis for chromosomal abnormalities in prenatal detection: A prospective clinical studyHailong Huang, Yan Wang, Min Zhang, et al.

BMC Medical Genomics|December 21, 2022

Clinical findings and genetic analysis of patients with copy number variants involving 17p13.3 using a single nucleotide polymorphism array: a single-center experienceBin Liang, Donghong Yu, Wantong Zhao, et al.

International Journal of Clinical and Experimental Pathology|January 15, 2020

Identification of a novel pre-terminating mutation in human HBB gene as a cause of β0-thalassemia phenotypeLiangpu Xu, Meihuan Chen, Hailong Huang, et al.

Scientific Reports|July 15, 2024

Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary centerHuili Xue, Aili Yu, Lingji Chen, et al.

The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|September 6, 2023

Identification of a novel 91.5 kb-deletion (αα)FJ in the α-globin gene cluster using single-molecule real-time (SMRT) sequencingLiangpu Xu, Meihuan Chen, Junhao Zheng, et al.

Genetics Research|June 17, 2025

Fujian Province β-Thalassemia: A Molecular and Hematological Study in Southeastern ChinaJunhao Zheng, Meihuan Chen, Siwen Zhang, et al.

Molecular Reproduction and Development|December 17, 2017

Application of the BACs-on-Beads™ assay for rapid prenatal detection application of BoBs™ for PND of aneuploidies and microdeletionsHailong Huang, Min Zhang, Yan Wang, et al.

Plos One|October 5, 2023

The clinical value of hsa-miR-190b-5p in peripheral blood of pediatric β-thalassemia and its regulation on BCL11A expressionMeihuan Chen, Xinrui Wang, Haiwei Wang, et al.

Pageof 4

Search research articles

Showing results (11-20 of 36) with videos related to