Qinghua H. Wu
Zhengzhou, 450052, China
Last Updated: 09/26/2026
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Found 32 publications
Prenatal diagnosis of a case with Schuurs-Hoeijmakers syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 31, 2023
Clinical characteristics and genetic analysis of a Chinese pedigree affected with Alström syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 29, 2023
Novel frameshift mutations in SALL4 in two Chinese families with Okihiro syndrome
Journal: Zhonghua yi xue za zhi
Published: July 12, 2023
Analysis of clinical features and FKTN gene variant in a child with congenital muscular dystrophy
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: July 10, 2022
Preliminary study on the role and mechanism of KIRREL3 in the development of esophageal squamous cell carcinoma.
Journal: Pathology, research and practice
Published: May 10, 2022
Variation analysis of genes associated with Usher syndrome type 1 in 136 Chinese deafness families
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
Published: March 18, 2021
Analysis of MYO15A variation in children with DFNB3
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: September 28, 2020
Genetic testing and prenatal diagnosis for two families affected with Joubert syndrome
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: April 27, 2020
Mutational analysis and prenatal diagnosis of TMPRSS3 gene in two Chinese families affected with deafness
Journal: Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery
Published: April 21, 2020
Analysis of genetic variation in patients with Waardenburg syndrome type Ⅱ by next generation sequencing
Journal: Zhonghua yi xue za zhi
Published: April 03, 2020
Prenatal diagnosis for two families affected with cleidocranial dysplasia due to novel RUNX2 variants
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: December 09, 2019
Identification of six novel variants in Waardenburg syndrome type II by next-generation sequencing.
Journal: Molecular genetics & genomic medicine
Published: September 13, 2019
Last Updated: 09/26/2026