Shuyuan Xue
Ueruemqi, China
Last Updated: 09/26/2026
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Found 8 publications
Beyond carrier frequency: a preliminary multicenter study of simultaneous couple-based comprehensive carrier screening for common and rare genetic disorders.
Journal: Genome medicine
Published: July 31, 2025
Clinical study of single nucleotide polymorphism-based chromosome microarray analysis in the etiological diagnosis of fetal congenital heart disease.
Journal: Scientific reports
Published: May 06, 2025
Evaluation of the clinical utility of NIPT-plus and analysis of adverse pregnancy outcomes.
Journal: Archives of gynecology and obstetrics
Published: May 22, 2024
Clinical application of chromosome microarray analysis and karyotyping in prenatal diagnosis in Northwest China.
Journal: Frontiers in genetics
Published: December 01, 2023
Clinical application of single nucleotide polymorphism microarray analysis in pregnancy loss in Northwest China.
Journal: Frontiers in genetics
Published: October 16, 2023
Spectrum analysis of inborn errors of metabolism for expanded newborn screening in Xinjiang, China.
Journal: PeerJ
Published: August 28, 2023
Prenatal diagnosis of partial deletion of NRXN1 gene with combined CNV-seq and qPCR assays
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: November 01, 2022
Showing 1-8 of 8
Last Updated: 09/26/2026