Xuemei Chen

Fujian Key Laboratory For Prenatal Diagnosis And Birth Defect
Fuzhou, China

Last Updated: 09/26/2026

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Found 28 publications

Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion Syndrome.

Ultrasound Phenotype, Genetic Analysis, and Pregnancy Outcomes of Fetuses With 1p36 Deletion Syndrome.

Journal: Molecular genetics & genomic medicine

Published: November 19, 2024

Regional patterns of genetic variants in expanded carrier screening: a next-generation sequencing pilot study in Fujian Province, China.

Regional patterns of genetic variants in expanded carrier screening: a next-generation sequencing pilot study in Fujian Province, China.

Journal: Frontiers in genetics

Published: November 13, 2024

Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center.

Prenatal genetic diagnosis of fetuses with dextrocardia using whole exome sequencing in a tertiary center.

Journal: Scientific reports

Published: January 31, 2024

Genetic analysis of chorionic villus tissues in early missed abortions.

Genetic analysis of chorionic villus tissues in early missed abortions.

Journal: Scientific reports

Published: September 23, 2023

Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing.

Genetic testing for fetal loss of heterozygosity using single nucleotide polymorphism array and whole-exome sequencing.

Journal: Scientific reports

Published: July 03, 2023

Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions.

Genetic analysis, ultrasound phenotype, and pregnancy outcomes of fetuses with Xp22.33 or Yp11.32 microdeletions.

Journal: Journal of perinatal medicine

Published: May 05, 2023

Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China.

Non-invasive prenatal testing for the diagnosis of congenital abnormalities: Insights from a large multicenter study in southern China.

Journal: Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologica

Published: March 24, 2023

Analysis of retest reliability for pregnant women undergoing cfDNA testing with a no-call result.

Analysis of retest reliability for pregnant women undergoing cfDNA testing with a no-call result.

Journal: Molecular biology reports

Published: December 11, 2022

A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family.

A novel PLS1 c.981+1G>A variant causes autosomal-dominant hereditary hearing loss in a family.

Journal: Clinical genetics

Published: October 11, 2022

16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up.

16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-up.

Journal: BMC pregnancy and childbirth

Published: October 08, 2022

Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies.

Efficiency of expanded noninvasive prenatal testing in the detection of fetal subchromosomal microdeletion and microduplication in a cohort of 31,256 single pregnancies.

Journal: Scientific reports

Published: September 11, 2022

Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience.

Fetal genetic findings by chromosomal microarray analysis and karyotyping for fetal growth restriction without structural malformations at a territory referral center: 10-year experience.

Journal: BMC pregnancy and childbirth

Published: August 04, 2022

Showing 1-12 of 28

Last Updated: 09/26/2026