Yuan Lv
Shenyang, China
Last Updated: 09/26/2026
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Found 21 publications
Prenatal exome sequencing of fetuses with central nervous system anomalies based on prenatal ultrasound and magnetic resonance imaging diagnosis: A retrospective cohort study with a systematic review and meta-analysis.
Journal: Acta obstetricia et gynecologica Scandinavica
Published: June 27, 2025
Incremental yield of prenatal exome sequencing in fetuses with skeletal system abnormalities: A systematic review and meta-analysis.
Journal: Acta obstetricia et gynecologica Scandinavica
Published: June 08, 2024
Comparison of the 2009 Institute of Medicine and 2021 Chinese guidelines for gestational weight gain: A retrospective population-based cohort study.
Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics
Published: December 02, 2022
First case of endometrial cancer after yolk sac tumor in a patient with Li-Fraumeni syndrome.
Journal: BMC women's health
Published: June 06, 2022
Acute Lymphoblastic Leukemia in Combined Methylmalonic Acidemia and Homocysteinemia (cblC Type): A Case Report and Literature Review.
Journal: Frontiers in genetics
Published: January 17, 2022
Fetal growth velocity references from a Chinese population-based fetal growth study.
Journal: BMC pregnancy and childbirth
Published: May 10, 2021
MiR-130a-5p/Foxa2 axis modulates fetal lung development in congenital diaphragmatic hernia by activating the Shh/Gli1 signaling pathway.
Journal: Life sciences
Published: September 16, 2019
A small supernumerary marker chromosome resulting in mosaic partial tetrasomy 4q26-q31.21 in a foetus with multiple congenital malformations.
Journal: Journal of genetics
Published: April 05, 2019
Whole-exome sequencing identifies a donor splice-site variant in SMPX that causes rare X-linked congenital deafness.
Journal: Molecular genetics & genomic medicine
Published: January 21, 2019
Compound heterozygous mutation of MUSK causing fetal akinesia deformation sequence syndrome: A case report.
Journal: World journal of clinical cases
Published: December 25, 2018
Screening of fetal chromosomal aneuploidy diseases using noninvasive prenatal testing in twin pregnancies.
Journal: Expert review of molecular diagnostics
Published: December 25, 2018
Novel compound heterozygous COG5 mutations in a Chinese male patient with severe clinical symptoms and type IIi congenital disorder of glycosylation: A case report.
Journal: Experimental and therapeutic medicine
Published: November 30, 2018
Last Updated: 09/26/2026