Hongdan Wang
NHC Key Laboratory Of Birth Defects Prevention
Zhengzhou, China
Zhengzhou, China
Last Updated: 09/26/2026
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Found 35 publications
Prenatal Diagnosis of COQ2 Variants in Suspected Coenzyme Q10 Deficiency.
Journal: Kidney international reports
Published: April 08, 2025
Whole-Brain Monosynaptic Inputs to Parasubthalamic Calretinin Neurons in Mice.
Journal: Molecular neurobiology
Published: February 18, 2025
Methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) gene polymorphisms and five related serum molecular levels in 2587 patients: Associated differentially with adverse pregnancy.
Journal: Molecular biology reports
Published: August 06, 2024
Correlation between maternal serum biomarkers and the risk of fetal chromosome copy number variants: a single-center retrospective study.
Journal: Archives of gynecology and obstetrics
Published: February 07, 2024
Genetic analysis of a Chinese pedigree with Cohen syndrome due to compound heterozygous variants of VPS13B gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 02, 2023
Analysis of a fetus with unbalanced translocation derived from a balanced t(6;14) maternal translocation
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: January 29, 2023
HNRNPC mediated m6A methylation of 5-methyltetrahydrofolate-homocysteine methyltransferase and involved in the occurrence of RSA.
Journal: Journal of reproductive immunology
Published: December 21, 2022
Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing.
Journal: Open life sciences
Published: November 09, 2022
Identification of a novel de novo mutation of SETBP1 and new findings of SETBP1 in tumorgenesis.
Journal: Orphanet journal of rare diseases
Published: June 22, 2022
Application of genomic copy number variation detection technology in prenatal diagnosis of 7617 pregnant women with serological screening abnormalities during the second trimester of pregnancy
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: May 22, 2022
A gonadal mosaicism novel KMT2D mutation identified by haplotype construction and clone sequencing strategy.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: March 18, 2022
Genetic Background of Kirgiz Ethnic Group From Northwest China Revealed by Mitochondrial DNA Control Region Sequences on Massively Parallel Sequencing.
Journal: Frontiers in genetics
Published: June 23, 2021
Last Updated: 09/26/2026