Xueyan Wang
Chengdu, China
Last Updated: 09/26/2026
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Found 13 publications
Structural Variation Sequencing of 26 Amniotic Fluid Samples With Partial Gene Duplications and Postnatal Follow-Up of the Fetuses.
Journal: Prenatal diagnosis
Published: January 06, 2026
A Prospective Evaluation of the Diagnostic Utility for Low-Coverage Genome Sequencing in Prenatal Samples: A Comparison With Chromosomal Microarray Analysis.
Journal: Prenatal diagnosis
Published: February 07, 2025
Clinical application value of targeted amplicon sequencing technology in fetuses with uniparental disomy-related imprinting disorders: a multicenter study.
Journal: Journal of translational medicine
Published: January 03, 2025
Performance evaluation of noninvasive prenatal testing on 24 chromosomes in a cohort of 118,969 pregnant women in Sichuan, China.
Journal: The Journal of international medical research
Published: September 16, 2024
Detection of variants IKBKG exon4-10 del and c.1167dupC using a novel gene-specific gap-PCR and long accurate-PCR in two families with incontinentia pigmenti.
Journal: Indian journal of dermatology, venereology and leprology
Published: August 13, 2024
Nephrogenic diabetes insipidus results from a novel in-frame deletion of AVPR2 gene in monozygotic-twin boys and their mother and grandmother.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: July 01, 2024
Delineation of an inverted tandem Xq23-26.3 duplication in a female featuring extremely short stature and mild mental deficiency.
Journal: Molecular cytogenetics
Published: September 28, 2023
Prenatal diagnosis of mosaic chromosomal aneuploidy and uniparental disomy and clinical outcomes evaluation of four fetuses.
Journal: Molecular cytogenetics
Published: September 28, 2023
Assessment of Combined Karyotype Analysis and Chromosome Microarray Analysis in Prenatal Diagnosis: A Cohort Study of 3710 Pregnancies.
Journal: Genetics research
Published: June 16, 2022
Identification of an SRY-negative 46,XX infertility male with a heterozygous deletion downstream of SOX3 gene.
Journal: Molecular cytogenetics
Published: October 24, 2021
Verification of a cryptic t(Y;15) translocation in a male with an apparent 45,X karyotype.
Journal: Molecular cytogenetics
Published: August 21, 2021
Application of quantitative fluorescencet-PCR in the prenatal diagnosis of chromosomale aneuploidies
Application of quantitative fluorescencet-PCR in the prenatal diagnosis of chromosomale aneuploidies
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 14, 2018
Last Updated: 09/26/2026