Wenxia Song

38 Weiyuanmen Road
Changzhi, 046000, China

Last Updated: 09/26/2026

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Found 16 publications

Prenatal SNP-array chromosomal microarray analysis in 3,549 pregnancies: indication-specific yields and clinical implications.

Prenatal SNP-array chromosomal microarray analysis in 3,549 pregnancies: indication-specific yields and clinical implications.

Journal: BMC pregnancy and childbirth

Published: December 14, 2025

Machine learning and SHAP-based risk assessment of PICC-related bloodstream infections in premature infants at the time of clinical suspicion.

Machine learning and SHAP-based risk assessment of PICC-related bloodstream infections in premature infants at the time of clinical suspicion.

Journal: Pediatric research

Published: November 20, 2025

Evidence of the correlation between air pollution and different types of birth defects: based on a distribution-lag non-linear model.

Evidence of the correlation between air pollution and different types of birth defects: based on a distribution-lag non-linear model.

Journal: Frontiers in public health

Published: January 29, 2025

Newborn screening for inherited metabolic disorders in central China: a retrospective study of 153,956 infants using non-derivatized tandem mass spectrometry.

Newborn screening for inherited metabolic disorders in central China: a retrospective study of 153,956 infants using non-derivatized tandem mass spectrometry.

Journal: Scientific reports

Published: January 08, 2025

Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patients.

Uncovering genetic contributors to developmental delay and intellectual disability: a focus on CNVs in pediatric patients.

Journal: Frontiers in genetics

Published: December 05, 2024

Novel ACAD8 variants identified in Isobutyryl-CoA dehydrogenase deficiency: challenges in phenotypic variability and management.

Novel ACAD8 variants identified in Isobutyryl-CoA dehydrogenase deficiency: challenges in phenotypic variability and management.

Journal: Frontiers in genetics

Published: November 22, 2024

Novel GJB2 mutation c.188delT compound with c.235delC causing non-syndromic hearing loss in a Chinese family: A case report.

Novel GJB2 mutation c.188delT compound with c.235delC causing non-syndromic hearing loss in a Chinese family: A case report.

Journal: Medicine

Published: August 16, 2024

Novel JAG1 variants leading to Alagille syndrome in two Chinese cases.

Novel JAG1 variants leading to Alagille syndrome in two Chinese cases.

Journal: Scientific reports

Published: September 30, 2023

Heterozygous deletion of HOXC10-HOXC9 causes lower limb abnormalities in congenital vertical talus.

Heterozygous deletion of HOXC10-HOXC9 causes lower limb abnormalities in congenital vertical talus.

Journal: Journal of medical genetics

Published: September 22, 2023

A GATA3 gene mutation that causes incorrect splicing and HDR syndrome: a case study and literature review.

A GATA3 gene mutation that causes incorrect splicing and HDR syndrome: a case study and literature review.

Journal: Frontiers in genetics

Published: July 07, 2023

Novel HPD mutation p.A244V compound with p.T219M causing tyrosinemia type III in a Chinese girl and review of the genotype-phenotype spectrum.

Novel HPD mutation p.A244V compound with p.T219M causing tyrosinemia type III in a Chinese girl and review of the genotype-phenotype spectrum.

Journal: Molecular genetics & genomic medicine

Published: June 16, 2023

Typical pantothenate kinase-associated neurodegeneration caused by compound heterozygous mutations in PANK2 gene in a Chinese patient: a case report and literature review.

Typical pantothenate kinase-associated neurodegeneration caused by compound heterozygous mutations in PANK2 gene in a Chinese patient: a case report and literature review.

Journal: Frontiers in neurology

Published: February 21, 2023

Showing 1-12 of 16

Last Updated: 09/26/2026