Huasha B. Zeng
Nanjing, 210004, China
Last Updated: 09/26/2026
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Found 8 publications
Genetic results and clinical outcome of fetuses with cardiac rhabdomyoma including a novel mutation in TSC2 gene.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: March 10, 2025
A Novel EBP c.452A>G Mutation Identified in a Girl with Conradi-Hünermann-Happle Syndrome Presenting with Hydronephrosis.
Journal: The application of clinical genetics
Published: January 16, 2025
Optical Genome Mapping for Chromosomal Aberrations Detection-False-Negative Results and Contributing Factors.
Journal: Diagnostics (Basel, Switzerland)
Published: December 06, 2023
Next-generation sequencing for genetic testing of hearing loss populations.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: July 14, 2023
Identification of two novel DNAJC12 gene variants in a patient with mild hyperphenylalaninemia.
Journal: Gene
Published: February 16, 2023
Genetic analysis of a novel SUMF1 variation associated with a late infantile form of multiple sulfatase deficiency.
Journal: Journal of clinical laboratory analysis
Published: August 01, 2022
Methylophiopogonanone a Inhibits LPS/ATP-Induced Macrophage Pyroptosis via ROS/NLRP3 Pathway
Journal: Molekuliarnaia biologiia
Published: May 05, 2022
OSBPL2-disrupted pigs recapitulate dual features of human hearing loss and hypercholesterolaemia.
Journal: Journal of genetics and genomics = Yi chuan xue bao
Published: March 12, 2019
Showing 1-8 of 8
Last Updated: 09/26/2026