Hongyan F. Wu

Xinxiang, 453003, China

Last Updated: 09/26/2026

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Found 8 publications

Discovery and comprehensive analysis of a congenital chimerism via paternity testing using short tandem repeat genotyping.

Discovery and comprehensive analysis of a congenital chimerism via paternity testing using short tandem repeat genotyping.

Journal: International journal of legal medicine

Published: September 12, 2024

Genetic inconsistency at the D6S1043 locus caused by microdeletion at 6q15.

Genetic inconsistency at the D6S1043 locus caused by microdeletion at 6q15.

Journal: International journal of legal medicine

Published: April 06, 2023

Retraction Note to: Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypes.

Retraction Note to: Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypes.

Journal: Human genetics

Published: December 11, 2021

Gastrointestinal leiomyoma with interstitial cells of Cajal: mimicker of gastrointestinal stromal tumor

Gastrointestinal leiomyoma with interstitial cells of Cajal: mimicker of gastrointestinal stromal tumor

Journal: Zhonghua bing li xue za zhi = Chinese journal of pathology

Published: June 11, 2018

Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypes.

Revisiting the male genetic landscape of China: a multi-center study of almost 38,000 Y-STR haplotypes.

Journal: Human genetics

Published: December 08, 2016

Characterization of tissue chromogranin A (CgA) immunostaining and clinicohistopathological changes for the 125 Chinese patients with primary small cell carcinoma of the esophagus.

Characterization of tissue chromogranin A (CgA) immunostaining and clinicohistopathological changes for the 125 Chinese patients with primary small cell carcinoma of the esophagus.

Journal: Diseases of the esophagus : official journal of the International Society for Diseases of the Esophagus

Published: October 31, 2016

Identification of a discordant genotype at the D2S1338 locus between Identifiler Plus®16 kit and Power Plex®21 system kit.

Identification of a discordant genotype at the D2S1338 locus between Identifiler Plus®16 kit and Power Plex®21 system kit.

Journal: Journal of forensic and legal medicine

Published: January 21, 2016

Association between SNP309 and del1518 Polymorphism in MDM2 Homologue and Esophageal Squamous Cell Carcinoma Risk in Chinese Population of Shandong Province.

Association between SNP309 and del1518 Polymorphism in MDM2 Homologue and Esophageal Squamous Cell Carcinoma Risk in Chinese Population of Shandong Province.

Journal: Annals of clinical and laboratory science

Published: August 16, 2015

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Last Updated: 09/26/2026