Yanhui Liu
Dongguan, China
Last Updated: 09/26/2026
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Found 25 publications
Advance in research on cell-free fetal DNA for monogenic disorders
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 05, 2022
Research progress on screening of pregnancy-related diseases based on fetal cell free DNA
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 09, 2021
Clinical and genetic analysis of a novel CHD4 gene variant in a Chinese patient with Sifrim-Hitz-Weiss syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 10, 2021
Analysis of tissue from pregnancy loss and aborted fetus with ultrasound anomaly using subtelomeric MLPA and chromosomal array analysis.
Journal: 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
Published: August 20, 2020
Recent Advances in Understandings Towards Pathogenesis and Treatment for Intrauterine Adhesion and Disruptive Insights from Single-Cell Analysis.
Journal: Reproductive sciences (Thousand Oaks, Calif.)
Published: August 06, 2020
CNV profiles of Chinese pediatric patients with developmental disorders.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 24, 2020
A Novel CREBBP in-Frame Deletion Variant in a Chinese Girl with Atypical Rubinstein-Taybi Syndrome Phenotypes.
Journal: Journal of molecular neuroscience : MN
Published: July 02, 2020
Regulation of CRMP2 by Cdk5 and GSK-3β participates in sevoflurane-induced dendritic development abnormalities and cognitive dysfunction in developing rats.
Journal: Toxicology letters
Published: June 27, 2020
Two novel KCNA1 variants identified in two unrelated Chinese families affected by episodic ataxia type 1 and neurodevelopmental disorders.
Journal: Molecular genetics & genomic medicine
Published: May 03, 2020
Concurrent pathogenic variants in SLC6A1/NOTCH1/PRIMPOL genes in a Chinese patient with myoclonic-atonic epilepsy, mild aortic valve stenosis and high myopia.
Journal: BMC medical genetics
Published: April 08, 2020
In Vitro and In Vivo Osteogenesis Induced by Icariin and Bone Morphogenetic Protein-2: A Dynamic Observation.
Journal: Frontiers in pharmacology
Published: February 22, 2020
Last Updated: 09/26/2026