Degang Wang
Zhongshan, 528400, China
Last Updated: 09/26/2026
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Found 10 publications
Functional Validation of a Novel Deep Intronic IMPG2 Variant Causing Pseudoexon Activation in Retinitis Pigmentosa with Macular Involvement.
Journal: The application of clinical genetics
Published: October 18, 2025
A case of mosaicism involving trisomy 21, maternal uniparental isodisomy, and normal diploid cells: Challenges and reflections in prenatal diagnosis
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: October 10, 2025
Evaluating Chromosomal Mosaicism in Prenatal Diagnosis: The Complementary Roles of Chromosomal Microarray Analysis and Karyotyping.
Journal: Journal of clinical laboratory analysis
Published: November 01, 2024
Screening and Diagnosis of Rare Thalassemia Variants: Is Third-Generation Sequencing Enough?
Journal: Archives of pathology & laboratory medicine
Published: February 19, 2024
Chromosomal microarray analysis for prenatal diagnosis of uniparental disomy: a retrospective study.
Chromosomal microarray analysis for prenatal diagnosis of uniparental disomy: a retrospective study.
Journal: Molecular cytogenetics
Published: August 10, 2023
Case report: A case report and literature review of complete trisomy 9.
Journal: Frontiers in genetics
Published: June 16, 2023
Ten years' experience in prenatal diagnosis of α-thalassemia in a municipal hospital and retrospective analysis of ultrasonic abnormalities.
Journal: International journal of hematology
Published: May 18, 2023
Next-generation sequencing reveals a case of Norrie disease in a child with bilateral ocular malformation.
Journal: Frontiers in genetics
Published: February 06, 2022
Detection of partial deletion and mosaicism using quantitative fluorescent polymerase chain reaction: Case reports and a review of the literature.
Journal: Journal of clinical laboratory analysis
Published: October 21, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026