Yu'e Chen
Quanzhou, China
Last Updated: 09/26/2026
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Found 18 publications
Genetic evaluation and pregnancy outcome of fetuses with digestive system malformations: an eight-year single-center retrospective study.
Journal: Frontiers in pediatrics
Published: January 29, 2026
Prenatal diagnosis and genetic assessment of fetuses with single umbilical artery using chromosomal microarray analysis: a seven-year single-center retrospective study.
Journal: BMC pregnancy and childbirth
Published: January 05, 2025
Case Report: Prenatal diagnosis of novel compound heterozygous variants in WDR35 gene causing short-rib thoracic dysplasia 7 with or without polydactyly.
Journal: Frontiers in pediatrics
Published: September 29, 2024
Molecular characterization of a rare TP63 variant associated with split-hand/split-foot malformation 4 and incomplete penetrance: disruption of the p63-Dlx signaling pathway.
Journal: BMC genomics
Published: April 15, 2024
Prenatal diagnosis and molecular cytogenetic analysis of pure chromosome 10p15.3 microdeletion using chromosomal microarray analysis.
Journal: BMC medical genomics
Published: February 04, 2024
Prenatal diagnosis of fetuses with 15q11.2 BP1-BP2 microdeletion in the Chinese population: a seven-year single-center retrospective study.
Journal: Molecular cytogenetics
Published: December 29, 2023
Molecular characterization of similar Hb Lepore Boston-Washington in four Chinese families using third generation sequencing.
Journal: Scientific reports
Published: October 05, 2023
Prenatal diagnosis and molecular cytogenetic characterization of fetuses with central nervous system anomalies using chromosomal microarray analysis: a seven-year single-center retrospective study.
Journal: Scientific reports
Published: September 30, 2023
Third-generation sequencing identified two rare α-chain variants leading to hemoglobin variants in Chinese population.
Journal: Molecular genetics & genomic medicine
Published: September 23, 2023
Prenatal diagnosis and molecular cytogenetic analysis of Xp22.31 microdeletions and microduplications in Chinese populations.
Journal: BMC pregnancy and childbirth
Published: August 03, 2023
Prenatal whole exome sequencing identified two rare compound heterozygous variants in EVC2 causing Ellis-van Creveld syndrome.
Journal: Molecular genetics & genomic medicine
Published: April 04, 2023
Case Report: Novel compound heterozygous variants in CHRNA1 gene leading to lethal multiple pterygium syndrome: A case report.
Journal: Frontiers in genetics
Published: June 08, 2022
Last Updated: 09/26/2026