Yanmin Luo (Y Luo)

Publication Activity (10 Years)

Years Active: 2016-2024
Publications (10 Years): 11

Top Topics

Gestational Age

Top Venues

Prenatal diagnosis

Molecular genetics & genomic medicine

Molecular cytogenetics

This page only lists publications with an associated author ORCID identifier.

Publications

Shuting Xia, Yingnan Ye, Jialiu Liu, Hanfei Qiu, Minhuan Lin, Zhiming He, Linhuan Huang, Malie Wang, Yanmin Luo
The Role of MALAT1 in Regulating the Proangiogenic Functions, Invasion, and Migration of Trophoblasts in Selective Fetal Growth Restriction. Biomolecules 14 (8) (2024)
Shuting Xia, Yingnan Ye, Jialiu Liu, Hanfei Qiu, Minhuan Lin, Zhiming He, Linhuan Huang, Malie Wang, Yanmin Luo
The Role of MALAT1 in Regulating the Proangiogenic Functions, Invasion, and Migration of Trophoblasts in Selective Fetal Growth Restriction. Biomolecules 14 (8) (2024)
J Liu, Z He, S Lin, Y Wang, L Huang, X Huang, Yanmin Luo
Absence of heterozygosity detected by single-nucleotide polymorphism array in prenatal diagnosis. Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 57 (2) (2021)
Minhuan Lin, Jinzhu Chen, Bing Liao, Zhiming He, Shaobin Lin, Yanmin Luo
When a vesicular placenta meets a live fetus: case report of twin pregnancy with a partial hydatidiform mole. BMC pregnancy and childbirth 21 (1) (2021)
Jialiu Liu, Linhuan Huang, Zhiming He, Shao-Bin Lin, Ye Wang, Yanmin Luo
Clinical value of genetic analysis in prenatal diagnosis of short femur. Molecular genetics & genomic medicine 7 (11) (2019)
Shaobin Lin, Shanshan Shi, Linhuan Huang, Ting Lei, Danlei Cai, Wenlong Hu, Yi Zhou, Yanmin Luo
Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses? Molecular cytogenetics 12 (2019)
Zhiyong Zou, Linhuan Huang, Shao-Bin Lin, Zhiming He, Yanmin Luo
Unusual twinning: Additional findings during prenatal diagnosis of twin zygosity by single nucleotide polymorphism (SNP) array. Prenatal diagnosis 38 (6) (2018)
Shao-Bin Lin, Shanshan Shi, Yi Zhou, Yuanjun Ji, Peizhi Huang, Jianzhu Wu, Baojiang Chen, Yanmin Luo
Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions. Prenatal diagnosis 38 (6) (2018)
Zhiyong Zou, Linhuan Huang, Shaobin Lin, Zhiming He, Hui Zhu, Yi Zhang, Qun Fang, Yanmin Luo
Prenatal diagnosis of posterior fossa anomalies: Additional value of chromosomal microarray analysis in fetuses with cerebellar hypoplasia. Prenatal diagnosis 38 (2) (2018)
Yi Zhang, Linhuan Huang, Xuan Huang, Zhiming He, Shao-Bin Lin, Ye Wang, Lin Li, Yanmin Luo, Qun Fang
Chromosomal aberrations and CNVs in twin fetuses with cardiovascular anomalies: Comparison between monochorionic diamniotic and dichorionic diamniotic twins. Prenatal diagnosis 38 (5) (2018)
Hui Zhu, Shaobin Lin, Linhuan Huang, Zhiming He, Xuan Huang, Yi Zhou, Qun Fang, Yanmin Luo
Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction. Prenatal diagnosis 36 (7) (2016)